Caricamento...
MASA syndrome: new clinical features and linkage analysis using DNA probes.
We describe a two generation family in which two males have the X linked recessive MASA syndrome (mental retardation, aphasia, shuffling gait, and adducted thumbs). A third male in this family died at the age of 15 years from congenital hydrocephalus. In the present family cerebral abnormalities are...
Salvato in:
| Pubblicato in: | J Med Genet |
|---|---|
| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BMJ Publishing Group
1990
|
| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1017259/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2277384/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.27.11.688 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|