Hypopigmented skin patches in 17q21.31 microdeletion syndrome-Reference-Cited by-同舟云学术

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Hypopigmented skin patches in 17q21.31 microdeletion syndrome

Published:2014-01 Issue:1 Volume:23 Page:32-34
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Digilio Maria C.,Bernardini Laura,Capolino Rossella,Digilio Marina,Dentici Maria L.,Novelli Antonio,Dallapiccola Bruno

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics(clinical),General Medicine,Pathology and Forensic Medicine,Anatomy,Pediatrics, Perinatology, and Child Health

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The clinical phenotype of Koolen‐de Vries syndrome in Turkish patients and literature review;American Journal of Medical Genetics Part A;2023-04-13

2. Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders;BMC Medical Genomics;2021-06-09

3. The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant;European Journal of Human Genetics;2015-08-26

4. Vitiligo in the Koolen-de Vries or 17q21.31 microdeletion syndrome;Clinical Dysmorphology;2015-04

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