Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Michal Yahav"'
Autor:
Ellen Taub, Russell J. Ferland, Christopher A. Walsh, Valerie Drasinover, Limor Anteki, Rachel Straussberg, Lina Basel-Vanagaite, Gideon Rechavi, Mordechai Shohat, Nurit Magal, Anna Alkelai, Dani Bercovich, Amos J. Simon, Revital Attia, Tsviya Olender, Michal Yahav
Background: The molecular basis of autosomal recessive non-syndromic mental retardation (NSMR) is poorly understood, mostly owing to heterogeneity and absence of clinical criteria for grouping families for linkage analysis. Only two autosomal genes,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6ee8a911ba1455fa2d14a6eb0c58796d
https://europepmc.org/articles/PMC2563235/
https://europepmc.org/articles/PMC2563235/
Autor:
Lina Basel‐Vanagaite, Liora Muncher, Rachel Straussberg, Metsada Pasmanik‐Chor, Michal Yahav, Limor Rainshtein, Christopher A. Walsh, Nurit Magal, Ellen Taub, Valerie Drasinover, Hanna Shalev, Revital Attia, Gideon Rechavi, Amos J. Simon, Mordechai Shohat
Publikováno v:
Annals of Neurology; Aug2006, Vol. 60 Issue 2, p214-222, 9p
Autor:
G. Rechavi, Michal Yahav, Tsafra Ilan, Mordechai Shohat, Lily King, Daniel H. Cohn, Tamy Shohat
Publikováno v:
The American Journal of Human Genetics. (3):647-651
Linkage studies were performed in a large family with an autosomal dominant phenotype characterized by nephropathy and hypertension. In this family of Iraqi Jewish origin, the nephropathy develops into progressive renal failure. By performing a genom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e7712ab668f69a228dc06c640663f7b