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Array Comparative Genomic Hybridization (aCGH) Analysis in Prader–Willi Syndrome

Prader–Willi syndrome (PWS) is due to loss of paternally expressed genes in the 15q11–q13 region generally from a paternal 15q11–q13 deletion. The proximal deletion breakpoint in the 15q11–q13 region occurs at one of two sites located within either of two large duplicons allowing for identification...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Am J Med Genet A
Prif Awduron: Butler, Merlin G., Fischer, William, Kibiryeva, Nataliya, Bittel, Douglas C.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2008
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5438264/
https://ncbi.nlm.nih.gov/pubmed/18266248
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.32249
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