A de novo Proximal 6q Deletion Confirmed by Array Comparative Genomic Hybridization-Reference-Cited by-同舟云学术

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A de novo Proximal 6q Deletion Confirmed by Array Comparative Genomic Hybridization

Published:2010-02-01 Issue:1 Volume:30 Page:84-88
ISSN:2234-3806
Container-title:Annals of Laboratory Medicine
language:en
Short-container-title:Ann Lab Med

Author:

Woo Kwang-Sook¹,Kim Ji-Eun¹,Kim Kyung-Eun¹,Kim Myo-Jing²,Yoo Jae-Ho²,Ahn Hyun-Sook³,Shaffer Lisa G.⁴,Han Jin-Yeong¹

Affiliation:

1. Department of Laboratory Medicine, Dong-A University College of Medicine, Busan, Korea

2. Department of Pediatrics, Dong-A University College of Medicine, Busan, Korea

3. Department of Obstetrics & Gynecology, Dong-A University College of Medicine, Busan, Korea

4. Signature Genomic Laboratories, Spokane, WA, USA

Publisher

Annals of Laboratory Medicine

Subject

Biochemistry, medical,Clinical Biochemistry,General Medicine

Link

https://synapse.koreamed.org/pdf/10.3343/kjlm.2010.30.1.84

Reference25 articles.

1. New insights into the phenotypes of 6q deletions

2. (6;15) Translocation with loss of chromosome material in the patient and various chromosome aberrations in family members

3. Interstitial deletions of chromosome 6q: genotype-phenotype correlation utilizing array CGH

Cited by 7 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 phenotypic spectrum of proximal 6q deletions based on a large cohort derived from social media and literature reports;European Journal of Human Genetics;2018-06-08

2. Proximal Deletion of 6q Overlapping with Toriello-Carey Facial Phenotype: Prenatal Findings, Clinical Course, Differential Diagnosis, and Review;Molecular Syndromology;2017-11-29

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

4. Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1;European Journal of Human Genetics;2014-11-05

5. Endocrine phenotype of 6q16.1-q21 deletion involving SIM1 and Prader-Willi syndrome-like features;American Journal of Medical Genetics Part A;2013-08-16

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