Molecular definition of a region of chromosome 21 that causes features of the Down syndrome phenotype.
Year: 1990
Type: article
Source: PubMed
Authors: J R Korenberg, H Kawashima, S M Pulst, T Ikeuchi, N Ogasawara, K Yamamoto, S A Schonberg, R West, L Allen, E Magenis
Language: English
Field: Medicine
Domain: Health Sciences
Open Access status: closed
Funder: National Institutes of Health
OpenAlex ID: W1496791107
