The human homologue of the Drosophila melanogaster flightless-I gene (flil) maps within the Smith-Magenis microdeletion critical region in 17p11.2.

The Smith-Magenis syndrome (SMS) appears to be a contiguous-gene-deletion syndrome associated with a proximal deletion of the short arm of chromosome 17 in band p11.2. The spectrum of clinical findings includes short stature, brachydactyly, developmental delay, dysmorphic features, sleep disturbance...

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Detalhes bibliográficos
Main Authors: Chen, K S, Gunaratne, P H, Hoheisel, J D, Young, I G, Miklos, G L, Greenberg, F, Shaffer, L G, Campbell, H D, Lupski, J R
Formato: Artigo
Idioma:Inglês
Publicado em: 1995
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801336/
https://ncbi.nlm.nih.gov/pubmed/7825574
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