Evidence for locus heterogeneity in human autosomal dominant split hand/split foot malformation.

Split hand/split foot (SHSF; also known as ectrodactyly) is a human developmental disorder characterized by missing central digits and other distal limb malformations. An association between SHSF and cytogenetically visible rearrangements of chromosome 7 at bands q21-q22 provides compelling evidence...

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Detalhes bibliográficos
Main Authors: Palmer, S. E., Scherer, S. W., Kukolich, M., Wijsman, E. M., Tsui, L. C., Stephens, K., Evans, J. P.
Formato: Artigo
Idioma:Inglês
Publicado em: 1994
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1918225/
https://ncbi.nlm.nih.gov/pubmed/7912888
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