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| Prof. Lihadh Al-Gazali | | | Professor in Clinical Genetics and Paediatrics | | Department of Paediatrics | | | Phone: | 971 3 7137 415 | | Fax: | 971 3 7672022 | | Email: | |
| Degree | University | Year | | MB ChB | Baghdad Medical College, Baghdad University | 1973 |
| | Postgraduate Diplomas, Certificates, and Fellowships | Year | | DCH, Royal College of Physicians, UK | 1979 | | MSc, Human Genetics, Edinburgh University, Edinburgh | 1983 | | MRCP, Paediatrics, Royal College of Physicians, Ireland | 1984 | | FRCP, Paediatrics, Royal College of Physicians, Ireland | 1993 | | FRCPCH, Royal College of Paediatrics and Child Health, UK | 1997 |
| | Appointment | Year | | Clinical research Fellow in Clinical Genetics, Leeds, UK | 1986-1990 | | Assisstant Professor in Clinical Genetics, FMHS, UAE University | 1990-1997 | | Associate Professor in Clinical Genetics, FMHS, UAEU | 1997-2003 |
| | Research Interests | | Clinical and Molecular delineation of recessive disorders in the Arab population |
| | Relevant Publications | Al-Gazali LI, Varghese M, Varady E, Al Talabani J, Scorer J, Bakalinova D. Neonatal Schwartz-Jampel Syndrome: A common AR syndrome in the UAE population. J Med Genet, 1996; 33: 203-211
Bayoumi R, Saar K, Nurnberg G, Reis A, Nur-E-Kamal M, Al-Gazali LI. Localization of a gene for an autosomal recessive syndrome of macrocephaly, multiple epiphyseal dysplasia (MED) and distinctive facies to chromosome 15q26.J Med Gene, 2001;38(6):369-373.
Kantarci S*, Al-Gazali L*, Hill R, Donnai D, Black G, Bieth E, Chassaing N, Lacombe D, Devriendt K, Teebi A, Loscertales M, Robson C, MacLaughlin DT, Noonan K, Russell M, Walsh C, Donahoe PK, Pober B. Mutations in megalin, a multiligand receptor, cause Donnai-Barrow syndrome and facio-oculo-acoustic-renal syndromes. Nat. Genet. 2007;39:957-959. Epub 2007 Jul 15 (* Co-1st author)
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