WDR11 is another causative gene for coloboma, cardiac anomaly and growth retardation in 10q26 deletion syndrome-Reference-Cited by-同舟云学术

WDR11 is another causative gene for coloboma, cardiac anomaly and growth retardation in 10q26 deletion syndrome

Published:2020-01 Issue:1 Volume:63 Page:103626
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Sutani Akito,Shima Hirohito,Hijikata Atsushi,Hosokawa Susumu,Katoh-Fukui Yuko,Takasawa Kei^ORCID,Suzuki Erina,Doi Shozaburo,Shirai Tsuyoshi,Morio Tomohiro,Fukami Maki^ORCID,Kashimada Kenichi

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference15 articles.

1. A subterminal deletion of the long arm of chromosome 10: a clinical report and review;Courtens;Am. J. Med. Genet.,2006

2. Craniosynostosis in 10q26 deletion patients: a consequence of brain underdevelopment or altered suture biology?;Faria;Am. J. Med. Genet.,2016

3. Deletion of the distal long arm of chromosome 10; is there a characteristic phenotype? A report of 15 de novo and familial cases;Irving;Am. J. Med. Genet.,2003

4. Genome-wide copy number analysis and systematic mutation screening in 58 patients with hypogonadotropic hypogonadism;Izumi;Fertil. Steril.,2014

5. The role of CHD7 and the newly identified WDR11 gene in patients with idiopathic hypogonadotropic hypogonadism and Kallmann syndrome;Kim;Mol. Cell. Endocrinol.,2011

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