Genetic screening for autosomal recessive nonsyndromic mental retardation in an isolated population in Israel
Open Access
- 6 December 2006
- journal article
- research article
- Published by Springer Nature in European Journal of Human Genetics
- Vol. 15 (2) , 250-253
- https://doi.org/10.1038/sj.ejhg.5201750
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardationJournal of Medical Genetics, 2005
- Non‐syndromic X‐linked mental retardation: From a molecular to a clinical point of viewJournal of Cellular Physiology, 2005
- A mutation in a novel ATP-dependent Lon protease gene in a kindred with mild mental retardationNeurology, 2004
- Prenatal diagnosis of Down syndrome: Ten year experience in the Israeli populationAmerican Journal of Medical Genetics Part A, 2003
- Truncating Neurotrypsin Mutation in Autosomal Recessive Nonsyndromic Mental RetardationScience, 2002
- The epidemiology of mental retardation: Challenges and opportunities in the new millenniumMental Retardation and Developmental Disabilities Research Reviews, 2002
- Fragile-X Carrier Screening and the Prevalence of Premutation and Full-Mutation Carriers in IsraelAmerican Journal of Human Genetics, 2001
- Trends in the frequencies of consanguineous marriages in the Israeli Arab communityClinical Genetics, 2000
- Consanguineous Matings in an Israeli-Arab CommunityArchives of Pediatrics & Adolescent Medicine, 1994
- Investigation of Families with Two or More Mentally Defective SiblingsA.M.A. Journal of Diseases of Children, 1959