Clinical and cytogenetic characterization of a boy with a de novo pure partial trisomy 16q24.1q24.3 and complex chromosome rearrangement

Saved in:
Bibliographic Details
Published inAmerican journal of medical genetics. Part A Vol. 161A; no. 4; pp. 897 - 900
Main Authors Zhou, Yang, Yao, Qi, Cui, Ying-Xia, Yao, Bing, Fan, Kai, Xia, Xin-Yi, Hu, Yu-An, Li, Xiao-Jun
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.04.2013
Wiley Subscription Services, Inc
Subjects
Child, Preschool
Chromosome Aberrations
Chromosome Banding
Chromosome Breakpoints
Chromosomes, Human, Pair 16 - genetics
Genetic Association Studies
Humans
In Situ Hybridization, Fluorescence
Male
Osteochondroma - diagnostic imaging
Osteochondroma - genetics
Radiography
Trisomy - diagnosis
Trisomy - genetics
Online AccessGet full text

Cover

More Information
Bibliography:Yang Zhou, Qi Yao, and Ying-Xia Cui contributed equally to this work.
How to Cite this Article: Zhou Y, Yao Q, Cui Y-X, Yao B, Fan K, Xia X-Y, Hu Y-A, Li X-J, 2013. Clinical and cytogenetic characterization of a boy with a de novo pure partial trisomy 16q24.1q24.3 and complex chromosome rearrangement. Am J Med Genet Part A 161A:897-900
ark:/67375/WNG-JBX3WHJX-R
National Natural Science Foundation of China - No. 30901652
ArticleID:AJMG35782
istex:CA933ADABBEE203BE20A405A8F8EB708BEC8D240
How to Cite this Article: Zhou Y, Yao Q, Cui Y‐X, Yao B, Fan K, Xia X‐Y, Hu Y‐A, Li X‐J, 2013. Clinical and cytogenetic characterization of a boy with a de novo pure partial trisomy 16q24.1q24.3 and complex chromosome rearrangement. Am J Med Genet Part A 161A:897–900
Yang Zhou, Qi Yao, and Ying‐Xia Cui contributed equally to this work.
ObjectType-Case Study-2
SourceType-Scholarly Journals-1
ObjectType-Feature-4
content type line 23
ObjectType-Report-1
ObjectType-Article-3
ISSN:1552-4825
1552-4833
DOI:10.1002/ajmg.a.35782