Terminal 2q deletion--a recognizable syndrome
Clin Genet
.
1997 Apr;51(4):290.
doi: 10.1111/j.1399-0004.1997.tb02475.x.
Authors
S L Wenger
,
L Y Boone
,
U Surti
,
M W Steele
PMID:
9184258
DOI:
10.1111/j.1399-0004.1997.tb02475.x
No abstract available
Publication types
Comment
Letter
MeSH terms
Abnormalities, Multiple / genetics*
Chromosome Deletion*
Chromosomes, Human, Pair 2*
Humans
Infant, Newborn
Syndrome