Homozygous MED25 mutation implicated in eye–intellectual disability syndrome-Reference-Cited by-同舟云学术

Homozygous MED25 mutation implicated in eye–intellectual disability syndrome

Published:2015-03-20 Issue:6 Volume:134 Page:577-587
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Basel-Vanagaite Lina,Smirin-Yosef Pola,Essakow Jenna Lee,Tzur Shay,Lagovsky Irina,Maya Idit,Pasmanik-Chor Metsada,Yeheskel Adva,Konen Osnat,Orenstein Naama,Weisz Hubshman Monika,Drasinover Valerie,Magal Nurit,Peretz Amit Gaby,Zalzstein Yael,Zeharia Avraham,Shohat Mordechai,Straussberg Rachel,Monté Didier,Salmon-Divon Mali,Behar Doron M.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-015-1541-x.pdf

Reference33 articles.

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3. Basel-Vanagaite L, Taub E, Halpern GJ et al (2006b) Genetic screening for autosomal recessive nonsyndromic mental retardation in an isolated population in Israel. Eur J Hum Genet 15:250–253. doi: 10.1038/sj.ejhg.5201750

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