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Clinical and Cytogenetic Survey of 39 Individuals With Prader-Labhart-Willi Syndrome
In a clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome (PLWS) (23 males and 16 females ranging in age from 2 weeks to 39 years), an interstitial deletion of chromosome 15 (breakpoints q11 and q13) was identified in 21 cases and apparently normal chromosomes in the...
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| Publicado no: | Am J Med Genet |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
1986
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5494992/ https://ncbi.nlm.nih.gov/pubmed/3953677 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.1320230307 |
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