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...

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Bibliografiske detaljer
Udgivet i:Dev Med Child Neurol
Main Authors: Fear, C. N., Mutton, D. E., Berry, A. C., Heckmatt, J. Z., Dubowitz, V.
Format: Artigo
Sprog:Inglês
Udgivet: Blackwell Publishing Ltd 2008
Fag:
Original Article
Online adgang: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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