WDR11 is another causative gene for coloboma, cardiac anomaly and growth retardation in 10q26 deletion syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference15 articles.
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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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