Work

Concurrent diagnoses of Prader–Willi syndrome and GM2 gangliosidosis caused by uniparental disomy of chromosome 15

Year: 2015

Type: article

Source: American Journal of Medical Genetics Part A

DOI: 10.1002/ajmg.a.37090

Authors: Debra S. Regier, Eyby Leon, Debra R. Counts, Cynthia J. Tifft, Dina J. Zand

Institutions: National Institutes of Health, National Human Genome Research Institute, Children's National, University of Maryland Medical Center

Language: English

Topic: Genetic Syndromes and Imprinting

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2071897688

FWCI:

Cites: 12

Cited by: 6

Related to: 10