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Maxillofacial dysostosis.

Four individuals in a single family affected with maxillofacial dysostosis are reported. Maxillary hypoplasia, delayed onset of speech, and poor development of language skills without associated hearing loss are the main characteristics of the syndrome which is transmitted as an autosomal dominant....

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Escobar, V, Eastman, J, Weaver, D, Melnick, M
Aineistotyyppi: Artikkeli
Kieli:English
Julkaistu: 1977
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1013620/
https://ncbi.nlm.nih.gov/pubmed/592352
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