Recombinant Chromosome 4 with Partial 4p Deletion and 4q Duplication Inherited from Paternal Pericentric Inversion-Reference-Cited by-同舟云学术

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Recombinant Chromosome 4 with Partial 4p Deletion and 4q Duplication Inherited from Paternal Pericentric Inversion

Published:2010-02-01 Issue:1 Volume:30 Page:89-92
ISSN:2234-3806
Container-title:Annals of Laboratory Medicine
language:en
Short-container-title:Ann Lab Med

Author:

Mun Se Jin¹,Cho Eun Hae²,Chey Myoung-Jae³,Shim Gyu-Hong³,Shin Bo-Moon¹,Lee Rae-Kyung¹,Ko Ji-Kyung⁴,Yoo Soo Jin¹

Affiliation:

1. Department of Laboratory Medicine, Sanggye Paik Hospital, Inje University College of Medicine, Seou, Koreal

2. Greencross Reference Laboratory, Yongin, Korea

3. Department of Pediatrics, Sanggye Paik Hospital, Inje University College of Medicine, Seoul, Korea

4. Department of Obstetrics and Gynecology, Sanggye Paik Hospital, Inje University College of Medicine, Seoul, Korea

Funder

Inje University

Publisher

Annals of Laboratory Medicine

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

Link

https://synapse.koreamed.org/pdf/10.3343/kjlm.2010.30.1.89

Reference17 articles.

1. First known microdeletion within the Wolf-Hirschhorn syndrome critical region refines genotype-phenotype correlation

2. Comparing Two Diagnostic Laboratory Tests for Several Microdeletions Causing Mental Retardation Syndromes: Multiplex Ligation-Dependent Amplification vs Fluorescent In Situ Hybridization

3. Wolf–Hirschhorn syndrome facial dysmorphic features in a patient with a terminal 4p16.3 deletion telomeric to the WHSCR and WHSCR 2 regions

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. Recombinant chromosome 4 in two fetuses - case report and literature review;Molecular Cytogenetics;2018-08-22

2. Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature review;Molecular Cytogenetics;2013

3. Recombinant Chromosome 4 from a Familial Pericentric Inversion: Prenatal and Adulthood Wolf-Hirschhorn Phenotypes;Case Reports in Genetics;2013

4. The Wolf-Hirschhorn Syndrome in Fetal Autopsy - A Case Report -;The Korean Journal of Pathology;2011

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