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CHROMOSOME 15 IN PRADER‐WILLI SYNDROME
SUMMARY: Nineteen children with the clinical features of Prader‐Willi syndrome were karyotyped, using both routine Giemsa banding and high‐resolution techniques. Chromosome abnormalities involving chromosome 15 were found in 10, entirely normal chromosomes in five and for the remaining four the find...
Tallennettuna:
| Julkaisussa: | Dev Med Child Neurol |
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| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Blackwell Publishing Ltd
2008
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7163620/ https://ncbi.nlm.nih.gov/pubmed/4018424 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1469-8749.1985.tb04540.x |
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