M-banding characterization of a 16p11.2p13.1 tandem duplication in a child with autism, neurodevelopmental delay and dysmorphism-Reference-Cited by-同舟云学术

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M-banding characterization of a 16p11.2p13.1 tandem duplication in a child with autism, neurodevelopmental delay and dysmorphism

Published:2008-11 Issue:6 Volume:51 Page:608-614
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Behjati Farkhondeh,Shafaghati Yousef,Firouzabadi Saghar Ghasemi,Kahrizi Kimia,Bagherizadeh Iman,Najmabadi Hossein,Bint Susan,Ogilvie Caroline

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference19 articles.

1. Recent segmental duplications in the human genome;Bailey;Science,2002

2. Facilitated stimulus-response associative learning and long term memory in mice lacking the NTAN1 amidase of the N-end rule pathway;Balough;Brain Res.,2001

3. Amplification of a pseudogene cassette underlies euchromatic variation of 16p at the cytogenetic level;Barber;Hum. Genet.,1999

4. Identification par les bandes Q et G des anomalies chromosomiques dans les avortements spontanes;Boue;Ann. Genet.,1976

5. Chromosome anomalies as a cause of spontaneous abortion;Carr;Am. J. Obstet. Gynecol.,1967

Cited by 12 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. 16p11.2 Microduplication Syndrome with Increased Fluid in the Cisterna: Coincidence or Phenotype Extension?;Genes;2023-08-03

2. 16p13.11p11.2 triplication syndrome: a new recognizable genomic disorder characterized by optical genome mapping and whole genome sequencing;European Journal of Human Genetics;2022-04-07

3. Phenotypic and Evolutionary Consequences of Deletion, Duplication, and Triplication at 16p11.2;SSRN Electronic Journal;2018

4. Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome;Molecular Neurobiology;2016-10-28

5. CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens;Scientific Reports;2016-06

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