An Xp21.3p11.4 duplication observed in a boy with intellectual deficiency and speech delay and his asymptomatic mother-Reference-Cited by-同舟云学术

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An Xp21.3p11.4 duplication observed in a boy with intellectual deficiency and speech delay and his asymptomatic mother

Published:2013-07 Issue:7 Volume:97 Page:467-470
ISSN:1542-0752
Container-title:Birth Defects Research Part A: Clinical and Molecular Teratology
language:en
Short-container-title:Birth Defects Research Part A: Clinical and Molecular Teratology

Author:

Wu Lingqian¹,Liu Jing¹,Lv Weigang¹,Wen Juan¹,Xia Yan¹,Liang Desheng¹

Affiliation:

1. State Key Laboratory of Medical Genetics; Central South University; Changsha Hunan People's Republic of China

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/bdra.23118/fullpdf

Reference13 articles.

1. Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseases;Smith;Hum Mol Genet,2007

2. Deletion of the immunoglobulin domain of IL1RAPL1 results in nonsyndromic X-linked intellectual disability associated with behavioral problems and mild dysmorphism;Franek;Am J Med Genet A,2011

3. A de novo duplication of Xp11.22-p11.4 in a girl with intellectual disability, structural brain anomalies, and preferential inactivation of the normal X chromosome;Holden;Am J Med Genet A,2010

4. Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis;Honda;J Hum Genet,2010

5. Partial Xp duplication in a girl with dysmorphic features: the change in replication pattern of late-replicating dupX chromosome;Kokalj Vokac;Clin Genet,2002

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. Further Delineation of Duplications of ARX Locus Detected in Male Patients with Varying Degrees of Intellectual Disability;International Journal of Molecular Sciences;2022-03-13

2. Prenatal Diagnosis of Sex Chromosome Abnormalities;Genetic Disorders and the Fetus;2021-04-20

3. Xp22.33p22.12 Duplication in a Patient with Intellectual Disability and Dysmorphic Facial Features;Molecular Syndromology;2016-01-12

4. Prenatal Diagnosis of Sex Chromosome Abnormalities;Genetic Disorders and the Fetus;2015-11-23

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