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*