Partial uniparental disomy with mosaic deletion 13q in an infant with multiple congenital anomalies-Reference-Cited by-同舟云学术

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Partial uniparental disomy with mosaic deletion 13q in an infant with multiple congenital anomalies

Published:2013-07-29 Issue:9 Volume:161 Page:2393-2395
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Jobanputra V.¹,Wilson A.²,Shirazi M.¹,Feenstra H.³,Levy B.¹,Anyane-Yeboa K.²,Warburton D.²⁴

Affiliation:

1. Department of Pathology; Columbia University; New York New York

2. Department of Pediatrics; Children's Hospital of New York-Presbyterian; New York New York

3. Department of Genetics; St. Luke's-Roosevelt Hospital Center; New York New York

4. Department of Genetics and Development; Columbia University Medical Center; New York New York

Funder

National Center for Research Resources

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36040/fullpdf

Reference10 articles.

1. Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomy;Berend;Am J Med Genet,1999

2. Mosaic 22q13 deletions: Evidence for concurrent mosaic segmental isodisomy and gene conversion;Bonaglia;Eur J Hum Genet,2009

3. The 13q- syndrome: The molecular definition of a critical deletion region in band 13q32;Brown;Am J Hum Genet,1995

4. Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis;Conlin;Hum Mol Genet,2010

5. Mitotic recombination and uniparental disomy in Beckwith-Wiedemann syndrome;Cooper;Genomics,2007

Cited by 2 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. Mosaicism for structural non-centromeric autosomal rearrangements in disease-defined carriers: sex differences in the rearrangements profile and maternal age distributions;Molecular Cytogenetics;2017-05-19

2. Chromosome 13q deletion syndrome involving 13q31-qter: A case report;Molecular Medicine Reports;2017-04-03

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