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Molecular and cytogenetic studies of the Prader-Willi syndrome.
Twenty-seven subjects with the Prader-Willi syndrome (PWS) were studied. Sixteen (59%) had a cytogenetic deletion involving chromosome 15q11-13. Nine were non-deletional and two patients had structural rearrangements of chromosome 15: 47,XY, + del(15)(pter----q12), var(15)(p11) and 45,XX,t(14q15q)....
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| Publicado no: | J Med Genet |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
1991
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1017050/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1682493/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.28.10.649 |
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