A (9;17) translocation, 46 chromosomes. Repository identification No. GM-988
Cytogenet Cell Genet
.
1977;18(4):244.
doi: 10.1159/000130769.
Authors
C C Lin
,
A J Kavanagh
,
M M Aronson
,
A E Greene
,
L L Coriell
PMID:
872632
DOI:
10.1159/000130769
No abstract available
Publication types
Case Reports
Research Support, U.S. Gov't, P.H.S.
MeSH terms
Chromosome Aberrations*
Chromosomes, Human, 16-18*
Chromosomes, Human, 6-12 and X*
Humans
Infant, Newborn
Male
Translocation, Genetic*