Possible genetic carriers in the spherophakia-brachymorphia syndrome
Am J Hum Genet
.
1955 Dec;7(4):398-425.
Authors
H W KLOEPFER
,
J W ROSENTHAL
PMID:
13275462
PMCID:
PMC1716673
No abstract available
MeSH terms
Bone and Bones / abnormalities*
Congenital Abnormalities*
Heredity*
Heterozygote*
Humans
Lens, Crystalline / abnormalities*
Weill-Marchesani Syndrome*