پروفسور محمد حسن کریمی‌نژاد

 

Prof. Mohammad Hassan Kariminejad

 

General Information

Mohammad Hassan Kariminejad/ Mohammad H. Kariminejad/ MH. Kariminejad/

MH. Karimi-Nejad/ MH Karimi Nejad,

   DATE OF BIRTH: DOB. 13 November 1928

   PLACE OF BIRTH: Sirjan, Kerman

MARITAL STATUS: Married

PRESENT POSITION:

Prof. of Pathology & Genetics, Tehran University (Retired)

Head of Kariminejad-Najmabadi Pathology & Genetics Center

Editor of chief: Quarterly Journal of "Genetics in the 3rd Millenium"

EXECUTIVE POSITION:

President of Representative of Human Genetics Branch, Iranian Genetics Society

Executive Editor of Genetics in the 3rd Millenium

ADDRESS: # 2, 4th Street, Phase 3, Shahrak Gharb (Quds), Tehran 1466713713

TEL: (+9821) 88363952-5

FAX: (+9821) 88083575

E-mail: mhkariminejad@yahoo.com

              mhkariminejad@sina.tums.ac.ir

 

   DOB. Nov.13.1928; Sirjan Kerman, Married 3 daughters, five grand children.

Elementary & Junior High School: Bader Sirjan 1935-1946,

High School: Saadi, Isfahan 1946-1948, Founder of Literary association

General Secretary of wall newspaper «Payame Saadi»

MD degree: Tehran Medical School, Tehran University 1948-1954

Military Service: Sirjan 1955-1957

     Specialty: Surgical Pathology 1961, Tehran Medical School Pathology department

    Subspecialty: Pediatric Path., Karolinska Hospital Stockholm, Sweden, 1963

    Cytopatholog: School of Medicine, Tehran University, WHO supervision, 1965

 Human Genetics: WHO Training Course in Human Genetics for Med. School Teachers

 (Intermittent) Denmark 1968-1972

 Gynecological Pathology Mass General Hosp, Harvard University, Boston, 1971-1973.

 

Academic memberships:

   -Iranian Pathology Society (Executive member) since establishment in 1960

   -Iranian Genetic Society (Executive member) since establishment 1965

   -European Society of Human Genetics (ESHG 1972)

   -International Gynecological Path. Society (IGPS) 1977

   -American Society of Human Genetics (ASHG) 1990

      -President of Medical Genetics, IGS. Three periods 2002-2006

   -Founder & President of Iranian Neurogenetics Society 2006-present 

 

Academic Position:

     -Resident in Pathology Department, Medical School, Tehran University 1957-1961

          -Assistant Professor. Pathology Department, School of Medicine, Tehran University 1961-65

     -Associate Prof. Pathology Department, School of Medicine, Tehran University 1965-71

     -Professor Pathology, School of Medicine, Tehran University 1971

  -Member of Pathology Board, Tehran University 1976- 1980

  -Member of Board of Accreditation, Tehran University 1976- 1980

 

Honorary Memberships:

   -Iranian Pediatrics Society

   -International Gynecological & Obstetrics Society

   -Iranian Society of Fertility & Infertility

   -Iranian Society of Female Genital Cancer

   -Association of Iranian Physician and Dentistry in Germany (VIA) 17.May.2007

 

Awards:

   -Fellowship in Pediatric Pathology KaroliskaHospital Swedish NIB foundation 1962-63

   -Fellowship in Cytopathology Course, WHO: 1964

   -Fellowship in 4th Training Course in Human Genetics for Medical School

    Teachers 1968 and two refresher courses Oct.1970 and 1972, WHO Scholarship

   -Award for the best scientific book 1991, Tehran University Principle of Human Genetics

    and Hereditary Diseases

   -Surgical and Clinical Pathology Organization 2003

   -Ministry of Health, Treatment and Medical Education 2003

   -International Avicenna Award of Iranian Physician and Dentisty in Germany,

    (VIA), May. 2007

   -Kerman University of Medical Science   

   -Medical Council, Sirjan City                  

 

Teaching:

   -Tehran University of Medical Science, and other Universities including:

     Iran, Red Lion & Sword, Kerman (Afzalipoor); Ahvaz (Chamran)  

     Iran, Zahedan,Yazd, Qazvin, Medical Faculty. Islamic Azad University

     Behzisty (Welfare & Rehabilitation) University

 

Training:

   * More than 200 trainees:

      Specialists in Pediatrics, Gynecology & Obstetrics; Genetics, Pathology,

      Many Masters and B.C. graduates related to Genetics field.

   * Conducting numbers of theses and articles.

 

Foundation:

   * Pathology & Genetic Center 1970

   * Prenatal Diagnosis Department 1985

   * Iranian Down Syndrome Society 1991

   * Medical Genetic Department Kerman University of Med. Science 1993

   * Founder and editor in chief, Genetic in 3rd Millennium; March 2002

   * Neurogenetic Conservation Society 2003

   * Educational & Welfare Kerman Raad Organization 2003

   * Iranian Neurogenetic Society 2006 (Founder & President)

 

         Scientific Activity

             * Participation in International and National Congress or Symposium, Presenting oral presentation usually yearly 1-3 times abroad and quite frequently inside the Country

             * Organizing Regional and International monthly Symposium Seminar and annual Congress

             * National Seminar of trophoblast tumors, Women's Hospital, Autumn 1975

             * National Congress Advance in Gynecological diseases, Autumn 1976

             * International Congress of Ovarian tumors with contribution of Harward University   (Prof. RE. Scully), Tehran 1977

             * 1st International Congress of Iranian Neurogenetics Society Neurometabolic disorders   Mofid Hospital, Nov. 2007

             * 2nd International Congress of INGS, Neuromuscular disease Tehran Mofid Hospital, Nov. 2008

             * 3rd & 4th Annual meeting of INGS: Neurodegenerative & Advances inNeurogenetics 2009-2010

             * 44 monthly Clinical Genetics Symposium 1999-2007

             * 50 Monthly Neurogenetics Symposium, 2006-present

 

          Publication:

 More than 110 articles in National (Farsi) Journal with English abstract

            More than 70 articles in International (English) Journal

 

Articles: English

 1- MH. Kariminejad,MD:

    Intrauterine infection; Pathways of fetal and early neonatal infection.

    Review of the amniotic infection Syndrome in 105 autopsies of new and

    stillborn babies. ACTA MEDICA IRANICA 12: 85-100, 1969

 2- MH. Krimi-Nejad, MD, Movlavi MA., Nasserghodssi MA, Ghafoorzadeh DJ., Behjatnia Y.

    Gonadoblastoma Associated with mixed gonadal dysgenesis.

        American Journal of obstetrics and gynecology. 113: 410, 414, 1972

 3- Kariminejad MH., and Scully R.E. :

    Female Adnexal tumor of  probable wolffian origin. A distinctive pathology centity.

    CANCER . 31: 671-677, 1973

 4- Lehmann H., ALA F., Hedayat S., Montazemi K., Kariminejad MH., Lightman S.,

    Kopec Ae., Mourant AE., Teesdale P. and FRS., Tills D. :

    The hereditary  blood  factors  of  the Kurds of Iran. Philosophical trans actions of

     the Royal Society of London. 266: 195-205, 1973

 5- Kariminejad, MH., Parsa H., and Emami M.:

     Results of  X and Y body analysis by fluorescent technique in various projects

     Clinical Genetics 10 : 347, 1977

 6- Wenn RV., Kamberi IA., Vossough P., Kariminejad, MH.,  Torabee E.,

     Ayoughi F., Keyvanjah M. and Sarberi :

     Human Testesterone-Oestradiol. Binding Globulin in Health and Disease

     Acta Endocrinologica  84 : 850-859, 1977

 7- Kariminejad MH., MD.

    Study of Sex chromosome in infertile and Gonadal Dysgenetic Patients.

    Clinical Genetics 14: 296, 1978    

 8- Kariminejad, MH.,  Khajavi H., Gharavi MJ., Kariminejad R.

    Neu Laxova Syndrome : Report of case and comments

    American. Journal of Medical Genetics 28: 17-23, 1987

 9- Dabir Ashrafi H., Kariminejad MH., Behjatnia V., and Moghadami Tabrizi N.

    Vestibular Bulb Hypertrophy

    Medical Journal of the Islamic Republic of Iran 2: 71-73, 1988

 10- Kariminejad R. , Ghofrani M., Najafi A., Kariminejad MH. :

      Reconsideration of the Cat Eye Syndrome: Reciprocal translocation t (11,22)   

      leading to partial trisomy of 11q and 22

      Medical Journal of the Islamic Republic of Iran 3 : 83-86, 1989

 11- Kariminejad MH. , Kariminejad R., Ghofrani M., and Najafi A.

       Parental reciprocal traslocation t (11,22), leading to partial trisomy of  11 and 22

       Clinical Genetics 37: 369, 1990

 12- Kariminejad MH., Kariminejad R., Khodadad A., and Najafi A.

      An interstitial deletion of the short arm of chromosome 3

      Clinical Genetics 37: 369,1990

 13- Kariminejad MH., Sadjadi SH., Kariminejad M, Asgari S., and Sadeghi A.

      Comparison of Congenital abnormalities and presumed genetic disorders in

      2000 consanguineous and non related couples.  Clinical Genetics 40 : 166-168, 1991

 14- Kariminejad MH. Et al. :

      Fragile X (Martin Bell Syndrome) in an Iranian family with 8 affected members

      Am. Journal of Human  49: Oct. Supplement, 1991

 15- Kariminejad MH., et al. :

       Multiple Congenital Malformation in female with X; 3 balanced translocation,

      Am. Journal of Human Genetics, Washington  49: Oct. Supplement, 1991

 16- Kariminejad, MH., et al.

      Geographical distribution of b thalassemia Clinical Genetics 41 : 159, 1993

 17- Kariminejad A., Nilforaoushan MA., Shafeghati Y., Kariminejad MH.

      Baller-Gerald Syndrome :  A case of Craniosynostosis and unilateral radial aplasia

      and review of literature Iranian Journal of Medical Science 19 : 64-69, 1994

 18- Kariminejad A., Kariminejad R., Najafi H., and Kariminejad MH.

      Blephorophimosis Syndrome (BPES) and additional abnormalities in a female

      with a balanced X; 3 translocation  Clinical Dysmorphology  5 : 259-261, 1996

 19- Kariminejad MH. et al.

      X-Linked Hypohydrotic ectodermal dysplasia in a family with

      5 males and 3 females affected, Clinical Genetics 42: 172-174, 1996

 20- Kariminejad, A, Kariminejad MH, Shafaghati Y.

      New findings in a patient with distal 13q-  Clinical dysmorphology 7 : 1-2, 1997

 21- Kariminejad A., Lashkarian N., and KarimiNejad MH.

      Results of Cytogenetic Analysis of 521 Amniotic Fluid Cell Cultures

      (Amniocentesis Performed in Iran )

      Medical Journal of the Islaminc Republic of Iran 13 : (3) 161-166, 1999

 22- Kiani MA. BS. Shakibaie MR. PhD., & Kariminejad MH. MD

      A. 22,22 Robertsonian Translocation in a patient with repeated abortion

      Archive Iranian Medicine 3(3) : 151-153, 2000

 23- Najmabadi H., Sahebjam S., Kariminejad R., Saremi A.,Sahebjam F.,

       Shafeghati Y., Kariminejad MH. : 

      Short Man with 46, X. del (Yp) del (Yq) Karyotype and more distal Yq deletion

      Arch Irn Med: 3 (4) 204-206, 2000

 24- Feleki X., Najmabadi H., Kariminejad R., Christopoulos G., Kleanthous M.:

      Identification of a novel b° Thalassemia

      Mutation, codon 80/ 81 (-C) in an Iranian family Hemoglobin 24 (4)  319- 321 (2000).

 25- Shafeghati Y., MD., Kariminejad, MH.

       Epidemiology and relative Incidence of rare neurometabolic and neurogenetic disorders in

       IRAN Archives of  Iranian Medicine  4 : 02. April. 2001

 26- Najmabadi H., Kariminejad R., Sahebjam S., Pourfarzad F., Teimourian S.,

       Sahebjam F., Amirizadeh N., Kariminejad MH.

       The b Thalassemia Mutation Spectrum in the Iranian Population

       Hemoglobin 25 (3) 285 – 296, 2001

 27- Kariminejad MH., Meshkat MR., Sohbati, S., Rezaei T., Kariminejad R.,

       Najmabadi H., Sarfarazi M. :  Congenital Blindness : Report of

                 Leber Congenital Amaurosis in a large Iranian Kindred; Arch Irn Med.; 4 (4): 171-176, 2001.

 28- Kariminejad, MH, Najmabadi H, Zangeneh M, Kariminjead R:

      b Thalassemia and chromosomal aberrations

      Archives Iranian Medicine 5 (1) 2002

 29- Moslehi R., Kariminejad MH., Ghaffari V., and Narod S. :

       Analysis of BRCA1 and BRCA2 mutation in an Iranian family AJMG 117 : 304-305, 2003

 30- Almadani N., Farhan F., Afroozan F., Shafaghati Y., and Kariminejad MH. :

      A large multigeneration Iranian Family with Autosomal Dominant Larsen Syndrome

      Genetics in the 3rd Millennium   1: 107-109, 2003

 31- Kariminejad R., Zangeneh M., Azimi F., et al. and Kariminejad MH.

      Cytogenetic study of 224 Bone Marrow samples of suspected chronic Myelogeneous

      Leukaemia patients Genetics in the 3rd Millennium 1: 166-173, 2003

 32- Zangeneh M, Kariminejad R, et al. Kariminejad MH (2004)

      Cytogenetic analysis of 358 bone marrow samples of suspected acute

      Leukemia patients; Genetics in the 3rd Millennium Vol. 1 No.4  pp 255-256

 33- Daneshi A, Shafeghaty Y, Kariminejad MH, Khosravi A, Farhang F:

      Hereditary Bilateral Conductive Hearing Loss caused by total loss of ossicles

 34- Bozorgmehr B, Kariminejad R, Kariminejad MH

      Goldenhar Syndrome, Report of a case with left Central Facial Paresis and review of

      literature Genetic in 3rd Millenium 3: 3, 612-616, 2005 

          35- Najmabadi H, Ghomari A, Sahebjam F, Kariminejad R, Hadavi V, Khaitbi T, Samavat A,

               Mehdipour E,  Modell B, Kariminejad MH: Fourteen year experience of Prenatal Diagnosis

               of Thalassemia in Iran, Community Genetics 2006; 9: 93-97 

 36- Kariminejad MH., and Bita Bozorgmehr MD.

       Russel-Silver Syndrome (2006)

       Genetics in 3rd Millennium Vol. 4 No. 1  PP: 740-41

 37- Jafarieh H, et al and Kariminejad MH.

      Comparison of early and Mid trimester amniocentesis in 1459 cases (2006)

      Genetics in 3rd Millennium Vol. 4 No. 3  PP: 858-63

 38- Bozorgmehr B, Hadavi V, Kariminejad MH.

       Freeman-Steldon Syndrome: report of 6 cases (2006)

       Genetics in 3rd Millennium Vol. 4 No. 3  PP: 871-75

 39- Mirzazadeh M, Kariminejad A, Nabavi-Nia N.,

      Azimi F, Kariminejad MH. (2006)

      A case of complete tetraploidy in amniotic fluid culture with

      normal karyotype in the repeat Genetics in 3rd Millennium Vol. 4 No. 3  PP: 876-79, 2006

 40- Salipante Sy. Benson KF., Luty J., Hadavi V., Kariminejad R., Kariminejad MH., (2007)

       Double de Novo mutation of ELA2 in Cyclic and Severe Congenital Neuropenia.

       Human Mutation 0. – 8, 2007

 41-  Kariminejad R. et al and Kariminejad MH.

       Overview of Lipid Storage Disease and 16 years Experience of biochemical analysis

       and prenatal diagnosis, Genetics in the 3rd Millennium 2007, Vol 4. No. 4 PP 942-55

 42- Bozorgmehr B., Kariminejad A. Hadavi V., Kariminejad MH.

       Aarskog.Scott Syndrome: Report of 7 cases and review of literature

       Genetics in the 3rd Millennium, Vol 4. No. 4 PP 954-56, 2007

 43- Bozorgmehr B., Hadavi V., Kariminejad MH.

       Freedman Sheldon Syndrome: Report of 6 cases

       Genetics in the 3rd Millennium 2006, Vol 4. No. 3 PP 871-76

 44- Mirza-Zadeh M., Kariminejad A., Nabavi-Nia N., Azimi F., and Kariminejad MH.

                A case of complete tetraploidy in amniotic fluid culture with normal karyotype in the repeat

       Genetics in the 3rd Millennium, Vol 4. No. 3 PP 876-79, 2006

 45- Shafagati Y., Vakili GH., Roshandel M., Vakili L., Kariminejad R., Kariminejad MH.

     Clinical and Enzymatic Diagnosis of GM1-Gangliosidosis; A case report

       Int J endocrinol Metab 2007; 2: 99.104

 46- Roxana Kariminejad, et al & Kariminejad MH.

       Overview of Lipid Strorage disease and 16 years Experience of Biochemical analysis and

       Prenatal Diagnosis, in IRAN

       Genetic in 3rd Millennium Vol. 4. No. 4, PP: 942-953 Winter 2006

 47- Bozorgmehr B, Kariminejad A, Hadavi V, and Kariminejad MH.

       Aarskog-Scott Syndrome: Report of 7 cases and review of Literature

       Genetic in 3rd Millennium Vol. 4, No. 4, PP 954-956 Winter 2006

 48- Najmabadi H. et al and Kariminejad MH.

       Fourteen year Experience of Prenatal Diagnosis of Thalassemia in Iran

       Community Genetics 9: 93-97, 2006

 49- Bicknell LS. Et al. and Kariminejad MH.

       A Molecular and Clinical Study olf Larson Syndrome caused by Mutation in FLNB

       J Med. Genet Published on line 1st: 26 June. 2006

 50- Stephen J. et al and Kariminejad, MH.

       Bouble de Nevo Mutation of ElA2 in Cyclic and Severe Congenital Neuropenia

       Journal HUMU 0, 1-8, 2007

     51- Rezaie T., Kariminejad MH., Meshkat MR., Sohbati S., Kariminejad R.

      Najmabadi H., Sarfarazi M.: Genetic Screening of Laber Congenital Amourosis

      in a large consanguineous Iranian family ophtamic Genetics 2007; 28: 224-228

       52- Kariminejad R., Bozorgmehr B., Sadighi-Gilani MR., Almadani N., Kariminejad MH.

            Am. J. Med. Gene 2008 part A, 146A: 1977-79

       53- Kariminejad A., Bozorgmehr B., Ashrafi MR., Kariminejad MH.

           Skull defects, Alopecia, and distinctive facies:

           A new syndrome?

          Clin. Dysmorphol  2008, 17: 203-205

 54- Kariminejad A, Goodarzi P, Asghari-Roodsari A, Kariminejad M.H. 2009 Amelia, Cloft

       Lip and Holoprosencephaly: A distinct entity Am. J. Med Genet Part A 149A:2828-2831

 55- Aghabaiklooei A, Goodarzi P, Kariminejad M.H. 2009 Lung Hypoplasia and its        

     associated major congenital  

     abnormalities in perinatal death. Indian J. Ped. 76:1137-40

 56- Kariminejad A, Kariminejad R, Tzschach A, Ultman R, Ahmed A, Asghari Roodsari A,

      Salehpoor S, Afroozan F, Ropers H, Kariminejad M.H. (2009) Craniosynostosis in a patient

     with 2q37.3 deletion 5q34 duplication. Association of extra copy of MS X2 Am. J. Med.

     Genet part A 149:1544-1549

 57- Ashrafi M.H, Kariminejad A, Alizadeh H, Bozorgmehr B, Amoeisan S, Kariminejad M.H.

      2010 Am J Med Genet.

 58- Kariminejad A, Goodarzi P, Than LT, Wehnet MS

      Restrictive dermopathy: Molecular diagnosis of restrictive dermopahty in a stillborn fetus

      From a consanguineous Iranian family

      Sandi Med. Journal 30: 150-153, 2009.

 59- Kariminejad M.H, van Diggelen O.P. 2009 Result of 19 years collaborative study with

      Erasmus University clinical genetic center on metabolic disorders. Genetics in the 3rd

      Millennium Vol 7:3, pp 1735-7.

 60- Shafeghati Y, Kariminejad M.H, Almadani N, Afroozan F. (2009) Sphyngolipidosis in Iran,

      a diagnostic and therapeutic challenge in the past two decades, Genetics in the 3rd

      Millennium Vol 7:3, 1738.

 61- Kariminejad A, Kariminejad R, Tzschach    , Najafi H, Alischo A,  Mullman R, Ropers HH,

      Kariminejad MH. : 11q14.1-11q22.1 Deletion in a one year old male with minor

      Dysmorphic features. Am. J. Med Genet part A 152A: 2651-2655.

 62- Kariminejad A, Kariminejad R, Moshtagh A, Zangeneh M, Kariminejad MH,

      Neuenschwander S, Okoniewski M, Wey E, Schinzel A and Baumer A: Pericentric

      Inversion of chromosome 18 in patients leading to a phenotypically normal child with

      Segmental uniparental disomy 18, Eur. J of Genet (2011) 1-6.

 

      Books:

Two books in male, and female genital pathology, seven books in basics of pediatrics, Pathology and

Gynecology Principles of Human Genetics. The principles of Human Genetics and Hereditary disease was the winner of the best scientific book of the year award in 1991;       Tehran university

    * Founder and editor in chief

            Genetics in the 3rd Millennium, Quarterly Journal Founded March 2002

 

      Editorial board member:

* Journal of Reproduction & Infertility official publication of Iranian Society of

  Reproduction and infertility

* Modern Genetics, Official Journal of Iranian Genetics Society 2004

* Yakhteh Medical Journal (Quarterly)

* Iranian Journal of reproductive Medicine 1998

* Journal of Hamadan Medical Science University 1995

          * Journal of Kerman Medical Science University 1990

 

      EDUCATION:

 Elementary & Junior High School: Bader Sirjan 1935-1946,

 Senior High School: Saadi, Isfahan 1946-1948

 Medical Degree: Tehran Medical School, Tehran University 1948-1954

 

 Specialty:

       Anatomical Pathology: Department of Pathology, Tehran Medical School,

       Tehran University 1957-1961

 

  Human Genetics:

       WHO 4th Training Course in Human Genetics for Medical

       School Teachers, Copenhagen, 1968-1972

 

  Subspecialty:

  Pediatric Pathology: Dept. of Pathology, Pediatric Division, Karolinska Hospital,

  Stockholm, Sweden, 1962-1963

 

   Cytology WHO Course:

        Cancer Institute, Tehran Medial School, 1964

 

  Gynecological Pathology:

        Pathology Department, Massachussetts General Hospital,

   Harvard Medial School, Boston, 1971-1973.

 

POSITION HELD

AWARDS/ DISTINCTION/ HONOURS

NIB Fellowship: Pediatric Pathology 1962

WHO Fellowship: 4th Training Course in Human Genetics, Copenhagen, Denmark 1968

WHO Fellowship: Refresher Course in Human Genetics, Glostrup, Denmark 1970

WHO Fellowship: Gynecological Pathology, 1971-1973

WHO Fellowship: Refresher Course in Human Genetics, Odense, Denmark 1972

 

INTERESTS:

Writing, Teaching, Swimming and Traveling

 

Books:

Pathology of Male Genitalia 1970

Principles of Human Genetics 1971

Pathology of Female Genital Tract 1972

Hereditary Disease and Chromosomal Aberration 1973

Principles of Human Genetics and Hereditary Diseases 1st edition 1978

Principles of Human Genetics and Hereditary Diseases 2st edition 1991

Winner of award of Tehran University

Alphabet of Human Genetics 2001

 

Articles:

More than one hundred papers in National and international journals, a few of which are

original, namely:

Kariminejad MH: et al: Single umbilical artery associated with congenital abnormalities.

Journal of General Medicine 4: 302-307, 1965

 

Kariminejad MH: et al: Gonadoblastoma associated with Mixed Gonadal Dysgenesis

Am. Journal of Obstetrics & Gynecology 1972

 

Lehmann H., et al Kariminejad MH: The hereditary  blood  factors  of  the Kurds of Iran.

Philosophical transactions of the Royal Society of London. 266: 195-205, 1973

 

Kariminejad MH., and Scully R.E: Female adnexal tumor of probable Wolffian origin.

A distinctive pathology centity. Cancer Vol. 31, PP: 671-677, 1973

 

Kariminejad, MH.,  et al: Neu Laxova Syndrome : Report of case and comments

American. Journal of Medical Genetics 28: 17-23, 1987

 

Kariminejad R, and Kariminejad MH et al: Reconsideration of the Cat Eye Syndrome:

Reciprocal translocation t (11,22) leading to partial trisomy of 11q and 22

Medical Journal of the Islamic Republic of Iran Vol 3 no. 12 P: 83-86, 1989

 

Kariminejad MH. et al:

Parental reciprocal translocation t (11,22), leading to partial trisomy of  11 and 22

Clinical Genetics 37: 369, 1990

 

Kariminejad MH. et al:  

An interstitial deletion of the short arm of chromosome 3

Clinical Genetics 37: 369,1990

 

Kariminejad MH. et al:

Comparison of Congenital abnormalities and presumed genetic disorders in 2000 consanguineous

and non related couples.  Clinical Genetics 40 : 166-168, 1991

 

Kariminejad MH. Et al:

Fragile X (Martin Bell Syndrome) in an Iranian family with 8 affected members

8th International Congress of Human Genetics Washington, DC Oct. 1991

 

Kariminejad MH., et al:

Multiple Congenital Malformation in female with X; 3 balanced translocation,

8th International Congress of Human Genetics Washington, DC Oct. 1991

 

Kariminejad, MH., et al:

Geographical distribution of b thalassemia

Clinical Genetics 41: 159, May 1993

 

Kariminejad A., Kariminejad MH, et al:

Baller-Gerald Syndrome: A case of Craniosynostosis and unilateral radial aplasia

and review of literature Iranian Journal of Medical Science 19 : 64-69, 1994

 

Kariminejad A., Kariminejad MH, et al:

Blephorophimosis Syndrome (BPES) and additional abnormalities in a female

with a balanced X; 3 translocation  Clinical Dysmorphology, Vol.5 : 259-261, 1996

 

Kariminejad MH. et al.

X-Linked Hypohydrotic ectodermal dysplasia in a family with

5 males and 3 females affected, Clinical Genetics 42: 172-174, May 1994

 

Kariminejad, A,  Kariminejad MH, et al:

New findings in a patient with distal 13q- 

Clinical dysmorphology 7 : 1-2, 1997

 

K. Lagersledi, B.M. Carlberg R, Kariminejad MH. et al: Analysis of a 43.6 Kb deletion in a patient

with Hunter Syndrome (MPS II): Identification of a Fusion Transcript Including Sequences from the

Gene Wand The IDS Gene

 

Kiani MA. BS. Shakibaie MR. PhD., & Kariminejad MH. MD:

A. 22,22 Robertsonian Translocation in a patient with repeated abortion

Archive Iranian Medicine 3(3) : 151-153, 2000

 

Shafeghati Y., MD., Kariminejad, MH, et al:

Epidemiology and relative Incidence of rare neurometabolic and neurogenetic disorders in

IRAN Archives of Iranian Medicine, Vol: 4 : No: 2, April. 2001

 

Shafeghati MD., Kariminejad MH, et al: 

Incidence of rare Neurometabolic and Neurogenetic disorders in IRAN

Archives of Iranian Medicine Vol. 4. No. 2 April 2001

 

Najmabadi H., Kariminejad MH, et al:

The b Thalassemia Mutation Spectrum in the Iranian Population

Hemoglobin 25 (3) 285 – 296, 2001

 

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