GZF1 Mutations Expand the Genetic Heterogeneity of Larsen Syndrome-Reference-Cited by-同舟云学术

GZF1 Mutations Expand the Genetic Heterogeneity of Larsen Syndrome

Published:2017-05 Issue:5 Volume:100 Page:831-836
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Patel Nisha,Shamseldin Hanan E.,Sakati Nadia,Khan Arif O.,Softa Ameen,Al-Fadhli Fatima M.,Hashem Mais,Abdulwahab Firdous M.,Alshidi Tarfa,Alomar Rana,Alobeid Eman,Wakil Salma M.,Colak Dilek,Alkuraya Fowzan S.

Funder

King Abdulaziz City for Science and Technology

King Salman Center for Disability Research

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference17 articles.

1. Multiple congenital dislocations associated with characteristic facial abnormality;Larsen;J. Pediatr.,1950

2. Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis;Krakow;Nat. Genet.,2004

3. A molecular and clinical study of Larsen syndrome caused by mutations in FLNB;Bicknell;J. Med. Genet.,2007

4. Severe cardiac anomalies in sibs with Larsen syndrome;Strisciuglio;J. Med. Genet.,1983

5. Larsen syndrome in siblings with consanguineous parents;Topley;Clin. Dysmorphol.,1994

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