Linkage of an autosomal dominant clefting syndrome (Van der Woude) to loci on chromosome Iq

Van der Woude syndrome (VWS) is an autosomal dominant disorder in which affected individuals have one or more of the following manifestations: cleft lip, cleft palate, hypodontia, or paramedian lower-lip pits. VWS is a well-characterized example of a single-gene abnormality that disturbs normal cran...

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Bibliografski detalji
Glavni autori: Murray, J. C., Nishimura, D. Y., Buetow, K. H., Ardinger, H. H., Spence, M. A., Sparkes, R. S., Falk, R. E., Falk, P. M., Gardner, R. J. M., Harkness, E. M., Glinski, L. P., Pauli, R. M., Nakamura, Y., Green, P. P., Schinzel, A.
Format: Artigo
Jezik:Inglês
Izdano: 1990
Teme:
Original Articles
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1683619/
https://ncbi.nlm.nih.gov/pubmed/2309700
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