Ayala Laufer‐Cahana

Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: Cast a wide FISHing net!

Donna M. McDonald‐McGinn, Melissa K. Tonnesen, Ayala Laufer‐Cahana et al. · Genetics in Medicine · 2001 · 314 citations · Full text

Biology, Genotype-phenotype Association, Wide Fishing Net +6

Alagille syndrome inherited from a phenotypically normal mother with a mosaic 20p microdeletion

Ayala Laufer‐Cahana, Ian D. Krantz, Lynn Bason et al. · American Journal of Medical Genetics · 2002 · 94 citations · Full text

A large deletion mutation in the CFTR gene (3120+1Kbdel8.6Kb): A founder mutation in the Palestinian Arabs

Israela Lerer, Ayala Laufer‐Cahana, Jacob R. Rivlin et al. · Human Mutation · 1999 · 50 citations

Palestinian Arabs, Mendelian Disorder, Genetic Disorder +15

Cystic fibrosis mutations in Israeli Arab patients

Ayala Laufer‐Cahana, Israela Lerer, Michal Sagi et al. · Human Mutation · 1999 · 34 citations · Full text

Genetics, Genetic Epidemiology, Human Polymorphism +16

Patient with trisomy 9p and a hypoplastic left heart with a tricentric chromosome 9

Jennifer J.D. Morrissette, Ayala Laufer‐Cahana, Līvija Medne et al. · American Journal of Medical Genetics Part A · 2003 · 11 citations

Heart Failure, Cytogenetics, Genetics +19