Related references
Note: Only part of the references are listed.Characteristics of genetic diseases in consanguineous populations in the genomic era: Lessons from Arab communities in North Israel
S. A. Shalev
CLINICAL GENETICS (2019)
Marriage Patterns and Reproductive Decision-Making in the Inhabitants of a Single Muslim Village during a 50-Year Period
Joel Zlotogora et al.
HUMAN HEREDITY (2014)
Systematic Classification of Disease Severity for Evaluation of Expanded Carrier Screening Panels
Gabriel A. Lazarin et al.
PLOS ONE (2014)
A TCTN2 Mutation Defines a Novel Meckel Gruber Syndrome Locus
Ranad Shaheen et al.
HUMAN MUTATION (2011)
The fate of 12 recessive mutations in a single village
J. Zlotogora et al.
ANNALS OF HUMAN GENETICS (2007)
Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19
HF Seow et al.
NATURE GENETICS (2004)
Share Paper
