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A new recessive syndrome of unusual facies and multiple structural abnormalities.

Two sibs with a similar pattern of dysmorphic facial features and multiple structural abnormalities are reported. Both had a normal karyotype. The parents are first cousins and neither shows any stigmata of the disorder. In view of the consanguinity and pattern of malformations, autosomal recessive...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: Thakker, Y, Donnai, D
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 1991
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1015797/
https://ncbi.nlm.nih.gov/pubmed/1956065
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