טוען...
Is gestation in Prader-Willi syndrome affected by the genetic subtype?
BACKGROUND: Prader-Willi syndrome (PWS) is a complex genetic disorder with errors in genomic imprinting, generally due to a paternal deletion of chromosome 15q11-q13 region. Maternal disomy 15 (both 15s from the mother) is the second most common form of PWS resulting from a trisomic zygote followed...
שמור ב:
| Main Authors: | , , , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Springer US
2009
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2767487/ https://ncbi.nlm.nih.gov/pubmed/19760168 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10815-009-9341-7 |
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