Developmental Delay Caused by a Supernumerary Chromosome, Inv Dup (15), Identified by Fluorescent In Situ Hybridization-Reference-Cited by-同舟云学术

Developmental Delay Caused by a Supernumerary Chromosome, Inv Dup (15), Identified by Fluorescent In Situ Hybridization

Published:1995-04 Issue:4 Volume:34 Page:223-226
ISSN:0009-9228
Container-title:Clinical Pediatrics
language:en
Short-container-title:Clin Pediatr (Phila)

Author:

Abuelo Dianne¹,Mark Hon Fong Louie²,Bier Jo-Ann Blaymore³

Affiliation:

1. Division of Genetics, Department of Pediatrics, Rhode Island Hospital and Brown University School of Medicine, Providence, Rhode Island

2. Laboratory of Cytogenetics, FISH, and Genotoxicology, Department of Pathology, Rhode Island Hospital and Brown University School of Medicine, Providence, Rhode Island

3. Child Development Center, Department of Pediatrics, Rhode Island Hospital and Brown University School of Medicine, Providence, Rhode Island

Publisher

SAGE Publications

Subject

Pediatrics, Perinatology and Child Health

Link

http://journals.sagepub.com/doi/pdf/10.1177/000992289503400410

Reference12 articles.

1. Forty four probands with an additional ?marker? chromosome

2. A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man.

3. Diagnostic and Statistical Manual of Mental Disorders. 3rd ed. revised, 1987. Washington, DC: American Psychiatric Association.

4. Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization.

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1. The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13;Neurobiology of Disease;2010-05

2. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridizatio;Clinical Genetics;2005-05-11

3. Fluorescent in situ hybridization (fish) as an adjunct to conventional cytogenetics;Advances in Structural Biology;2000

4. Trisomy 9 in a Patient with Secondary Acute Myelogenous Leukemia Detected by Fluorescent in situ Hybridization;Pathobiology;1999

5. Autism and maternally derived aberrations of chromosome 15q;American Journal of Medical Genetics;1998-04-01