Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15
N Engl J Med
.
1992 Mar 19;326(12):807-11.
doi: 10.1056/NEJM199203193261206.
Authors
D F Smeets
1
,
B C Hamel
,
M R Nelen
,
H J Smeets
,
J H Bollen
,
A P Smits
,
H H Ropers
,
B A van Oost
Affiliation
1
Department of Human Genetics, University Hospital Nijmegen, The Netherlands.
PMID:
1538725
DOI:
10.1056/NEJM199203193261206
No abstract available
Publication types
Case Reports
MeSH terms
Alleles
Child, Preschool
Chromosome Deletion
Chromosomes, Human, Pair 15*
Chromosomes, Human, Pair 6*
Female
Humans
Male
Paternity
Prader-Willi Syndrome / genetics*
Translocation, Genetic*