Work

A male newborn with VACTERL association and Fanconi anemia with a FANCB deletion detected by array comparative genomic hybridization (aCGH)

Year: 2011

Type: article

Study design: Case Report

Source: American Journal of Medical Genetics Part A

DOI: 10.1002/ajmg.a.34296

Authors: Luis A. Umaña, Pilar Magoulas, Weimin Bi, Carlos A. Bacino

Institution: Baylor College of Medicine

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

OpenAlex ID: W2168082807

FWCI: 0.548

Cites: 21

Cited by: 15

Related to: 10