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Quoted phrase not found in phrase index: "Prader-Willi syndrome due to imprinting mutation"
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Autism spectrum disorder in Prader-Willi syndrome: A systematic review.
Bennett JA, Germani T, Haqq AM, Zwaigenbaum L. Bennett JA, et al. Am J Med Genet A. 2015 Dec;167A(12):2936-44. doi: 10.1002/ajmg.a.37286. Epub 2015 Aug 29. Am J Med Genet A. 2015. PMID: 26331980 Review.
Prader-Willi syndrome (PWS) is a rare genetic disorder that results from lack of expression of paternally-derived genes on chromosome 15q11-13; caused by a deletion (DEL), uniparental disomy (UPD), or a rare imprinting center defect. ...
Prader-Willi syndrome (PWS) is a rare genetic disorder that results from lack of expression of paternally-derived genes …
Prader-Willi-like phenotypes: a systematic review of their chromosomal abnormalities.
Rocha CF, Paiva CL. Rocha CF, et al. Genet Mol Res. 2014 Mar 31;13(1):2290-8. doi: 10.4238/2014.March.31.9. Genet Mol Res. 2014. PMID: 24737477 Free article. Review.
Prader-Willi syndrome (PWS) is caused by the lack of expression of genes located on paternal chromosome 15q11-q13. ...A search was carried out using the "National Center for Biotechnology Information" (www.pubmed.com) and "Scientific Electronic Library Online …
Prader-Willi syndrome (PWS) is caused by the lack of expression of genes located on paternal chromosome 15q11-q13. ...A …
Autism spectrum disorders in Prader-Willi and Angelman syndromes: a systematic review.
Veltman MW, Craig EE, Bolton PF. Veltman MW, et al. Psychiatr Genet. 2005 Dec;15(4):243-54. doi: 10.1097/00041444-200512000-00006. Psychiatr Genet. 2005. PMID: 16314754 Review.
Autism spectrum disorders (ASDs) have been linked with maternally derived duplications/triplications of chromosome 15q11-13 and therefore might occur more frequently in people with Prader-Willi syndrome (PWS) when due to uniparental disomy (UPD), than in othe …
Autism spectrum disorders (ASDs) have been linked with maternally derived duplications/triplications of chromosome 15q11-13 and therefore mi …