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Expanding the genotype–phenotype correlation in subtelomeric 19p13.3 microdeletions using high resolution clinical chromosomal microarray analysis

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Year: 2013
Type: article
Study design: Case Report
Source: American Journal of Medical Genetics Part A
DOI: 10.1002/ajmg.a.35886
Authors: Sirisha Peddibhotla, Mohamed Khalifa, Frank J. Probst, Jennifer Stein, Leslie L. Harris, Debra L. Kearney, Gail H. Vance, Marilyn J. Bull, Dorothy K. Grange, Gunter H. Scharer, Sue‐Hae L. Kang, Pawel Stankiewicz, Carlos A. Bacino, Sau W. Cheung, Ankita Patel
Institutions: Baylor College of Medicine, Akron Children's Hospital, Texas Children's Hospital, Indiana University Indianapolis, Indiana University School of Medicine, Indiana University Health, Riley Hospital for Children, St. Louis Children's Hospital, Washington University in St. Louis, Medical College of Wisconsin, University of Colorado Anschutz, University of Colorado Denver, Allina Health
Language: English

Topic: Genomic variations and chromosomal abnormalities
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funder: Centers for Disease Control and Prevention
OpenAlex ID: W2055809555
FWCI: 2.021
Cites: 15
Cited by: 60
Related to: 10
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