Rare presentation of 6q16.3 microdeletion syndrome with severe upper limb reduction defects and duodenal atresia-Reference-Cited by-同舟云学术

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Rare presentation of 6q16.3 microdeletion syndrome with severe upper limb reduction defects and duodenal atresia

Published:2017-04-26 Issue:6 Volume:5 Page:905-914
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Donahue Megan L.¹^ORCID,Rohena Luis O.²³

Affiliation:

1. Department of Pediatrics; San Antonio Military Medical Center; San Antonio Texas

2. Division of Medical Genetics; Department of Pediatrics; San Antonio Military Medical Center; San Antonio Texas

3. Department of Pediatrics; University of Texas Health Science Center at San Antonio; San Antonio Texas

Publisher

Wiley

Subject

General Medicine

Reference26 articles.

1. New insights into the phenotypes of 6q deletions;Hopkin;Am. J. Med. Genet.,1997

2. A de novo interstitial 6q deletion in a boy with a split hand malformation;Duran-Gonzalez;J. Appl. Genet.,2007

3. Three cases with de novo 6q imbalance and variable prenatal phenotype;Grati;Am. J. Med. Genet. A,2005

4. Interstitial deletion of the long arm of chromosome 6 associated with unusual limbanomalies: report of two new patients and review of the literature;Pandya;Am. J. Med. Genet.,1995

5. Further delineation of interstitial chromosome 6 deletion syndrome and review of the literature;Zherebtsov;Clin. Dysmorphol.,2007

Cited by 1 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. Case report: A new de novo 6q21q22.1 interstitial deletion case in a girl with cerebellar vermis hypoplasia and developmental delay and literature review;Frontiers in Genetics;2024-02-06

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