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Holt-Oram syndrome: a clinical genetic study.

A clinical and genetic study of the Holt-Oram syndrome (HOS) has been carried out in the United Kingdom involving 55 cases designated Holt-Oram syndrome, together with their parents and sibs. Data from the clinical assessment of both familial and isolated cases were used to define the HOS phenotype...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Newbury-Ecob, R A, Leanage, R, Raeburn, J A, Young, I D
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1996
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050579/
https://ncbi.nlm.nih.gov/pubmed/8730285
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