Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome-Reference-Cited by-同舟云学术

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Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome

Published:2004 Issue:1-2 Volume:107 Page:68-76
ISSN:1424-8581
Container-title:Cytogenetic and Genome Research
language:en
Short-container-title:Cytogenet Genome Res

Author:

Tadin-Strapps M.,Warburton D.,Baumeister F.A.M.,Fischer S.G.,Yonan J.,Gilliam T.C.,Christiano A.M.

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics,Molecular Biology

Cited by 20 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. Linked genetic variation and not genome structure causes widespread differential expression associated with chromosomal inversions;Proceedings of the National Academy of Sciences;2018-05-07

2. Selection on Inversion Breakpoints Favors Proximity to Pairing Sensitive Sites in Drosophila melanogaster;Genetics;2016-09-01

3. Disorders of Hair and Nails;Hurwitz Clinical Pediatric Dermatology;2016

4. Molecular cytogenetic characterization of a familial pericentric inversion 3 associated with short stature;European Journal of Medical Genetics;2015-03

5. A 11.7-Mb Paracentric Inversion in Chromosome 1q Detected in Prenatal Diagnosis Associated with Familial Intellectual Disability;Cytogenetic and Genome Research;2015

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