Prevalence and molecular characterization of Glucose-6-Phosphate dehydrogenase deficient variants among the Kurdish population of Northern IraqNasir Al-Allawi
Department of Pathology, College of Medicine, University of Dohuk, Azadi Hospital road, 1014 AM Dohuk, Iraq
BMC Blood Disord 10:6. 2010
..The aim of this study is to determine the prevalence of this enzymopathy and its molecular basis among Iraqi Kurds...
- Cockayne syndrome in 2 siblings
Hanan A Hamamy
National Center for Diabetes, Endocrinology and Genetics, Jordan University Hospital, Amman, Jordan
Saudi Med J 26:875-9. 2005
..The radiological findings of thinning of ribs and slender femora with narrow medullary canals have not previously been reported in this syndrome. We discuss the implications of these findings...
- Consanguinity and genetic disorders. Profile from Jordan
Hanan A Hamamy
National Center for Diabetes, Endocrinology and Genetics, Department of Pediatrics, Jordan University Hospital, Amman, Jordan
Saudi Med J 28:1015-7. 2007
..The objective of this study is to define the specific categories of genetic disorders associated with consanguineous marriages...
- Alstrom syndrome in four sibs from northern Jordan
Hanan Hamamy
National Center for Diabetes, Endocrinology, and Genetics, Amman, Jordan
Ann Saudi Med 26:480-3. 2006
- Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report
Hanan Hamamy
Department of Genetic Medicine and Development, University of Geneva Medical School, and University Hospitals of Geneva, Geneva, Switzerland
Genet Med 13:841-7. 2011
....
- Griscelli syndrome type 2: a rare and lethal disorder
Amira Masri
Department of Pediatrics, Division of Child Neurology, Jordan University Hospital, Amman, Jordan
J Child Neurol 23:964-7. 2008
..Mutation analysis in family members revealed the presence of a missense mutation in Rab27a gene. In addition to the rare presentation, this is the first case of Griscelli syndrome to be reported from Jordan...
- Jordan: communities and community genetics
Hanan Hamamy
National Center for Diabetes, Endocrinology and Genetics, Amman, Jordan
Community Genet 10:52-60. 2007
..The demographic data suggest that the health system in Jordan is capable of introducing some basic community genetic services into the primary health care program through comprehensive and cost-effective programs...
- Profile of developmental delay in children under five years of age in a highly consanguineous community: a hospital-based study--Jordan
Amira Masri
Department of Pediatrics, Division of Child Neurology, Faculty of Medicine, The University of Jordan, P O Box 1612, 11941 Amman, Jordan
Brain Dev 33:810-5. 2011
..To assess etiologies and risk factors for global developmental delay (GDD) in children...
- Familial short fifth metacarpals and insulin resistance
Muwafag Hyari
National Center for Diabetes, Endocrinology and Genetics, P.O. Box 13165, 11942 Amman, Jordan
Skeletal Radiol 35:702-5. 2006
..This constellation of findings has not been previously reported and could point to the presence of two disorders segregating in the family or to a novel syndrome with autosomal dominant inheritance and variable expressivity...
- Genetic disorders in the Arab world
Lihadh Al-Gazali
Department of Paediatrics, Faculty of Medicine and Health Sciences, United Arab Emirates University, Al-Ain, United Arab Emirates
BMJ 333:831-4. 2006
- Etiologies, outcomes, and risk factors for epilepsy in infants: a case-control study
Amira Masri
The University of Jordan, Faculty of Medicine, Pediatric Department, Division of Child Neurology, Jordan
Clin Neurol Neurosurg 110:352-6. 2008
..To determine the etiologies, outcomes, and risk factors for epilepsy in infants...
