A 4q21-q22 deletion in a girl with severe growth retardation
Clin Genet
.
2002 Mar;61(3):226-8.
doi: 10.1034/j.1399-0004.2002.610311.x.
Authors
N Harada
,
T Nagai
,
O Shimokawa
,
N Niikawa
,
N Matsumoto
PMID:
12000367
DOI:
10.1034/j.1399-0004.2002.610311.x
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Child
Child, Preschool
Chromosome Deletion*
Chromosomes, Human, Pair 4*
Female
Growth Disorders / genetics*
Humans
In Situ Hybridization, Fluorescence
Karyotyping