Phenotype of maternal UPD(14)
Am J Med Genet
.
1996 Dec 2;66(1):89.
doi: 10.1002/(SICI)1096-8628(19961202)66:1<89::AID-AJMG22>3.0.CO;2-L.
Authors
W P Robinson
,
S Langlois
PMID:
8957520
DOI:
10.1002/(SICI)1096-8628(19961202)66:1<89::AID-AJMG22>3.0.CO;2-L
No abstract available
Publication types
Comment
Letter
MeSH terms
Chromosome Aberrations*
Chromosomes, Human, Pair 14*
Female
Genomic Imprinting*
Humans
Male
Translocation, Genetic