Total: 1 |
|
PMID (PMCID) | ||
---|---|---|
9288098 |
MIXED_SAMPLE | |
Disruption of human limb morphogenesis by a dominant negative mutation in CDMP1. | ||
Thomas JT, Kilpatrick MW, Lin K, Erlacher L, Lembessis P, Costa T, Tsipouras P, Luyten FP. Nat Genet. 1997;17(1):58-64. |
||
Chondrodysplasia Grebe type (CGT) is an autosomal recessive disorder characterized by severe limb shortening and dysmorphogenesis. |