Further delineation of interstitial chromosome 6 deletion syndrome and review of the literature-Reference-Cited by-同舟云学术

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Further delineation of interstitial chromosome 6 deletion syndrome and review of the literature

Published:2007-07 Issue:3 Volume:16 Page:135-140
ISSN:0962-8827
Container-title:Clinical Dysmorphology
language:en
Short-container-title:

Author:

Zherebtsov Monica M.,Klein Rachel T.,Aviv Hana,Toruner Gokce A.,Hanna Nazeeh N.,Brooks Susan Sklower

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

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

Reference15 articles.

1. Identification of connexin-43 (alpha-1) gap junction gene mutations in patients withhypoplastic left heart syndrome by denaturing fradient gel electrophoresis (DGGE);Dasgupta;Mutat Res,2001

2. Deletion of the long arm of chromosome 6: two new patients and literature review;Evers;Clin Genet,1996

3. Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature;Gilhuis;Eur Paediatr Neurol Soc,2000

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

5. Interstitial deletion of the long arm of chromosome 6 associated with absent pulmonary valve;Horigome;Am J Med Genet,1991

Cited by 14 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

2. Clinical Features in Patients with Microdeletion at 6q14.1-q15;The Indian Journal of Pediatrics;2017-05-29

3. Rare presentation of 6q16.3 microdeletion syndrome with severe upper limb reduction defects and duodenal atresia;Clinical Case Reports;2017-04-26

4. Phenotypic variability in patients with interstitial 6q21-q22 microdeletion and Acro-Cardio-Facial syndrome;American Journal of Medical Genetics Part A;2016-05-18

5. Clinical and molecular characterization of a patient with interstitial 6q21q22.1 deletion;Molecular Cytogenetics;2015-04-28

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