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Genomics
- ... microdeletion 17q12 recurrent deletion syndrome Deletion 17q12 Recurrent genomic rearrangement in chromosome 17q12 Genetic Testing Registry: Chromosome ...
- ... specific gene activity results from a process called genomic imprinting.Most cases of Prader-Willi syndrome (about ...
- ... gene expression are caused by a phenomenon called genomic imprinting. Abnormalities involving genes on chromosome 11 that undergo genomic imprinting are responsible for most cases of Beckwith- ...
- ... difference in gene activation is a phenomenon called genomic imprinting. In some cases of Wilms tumor, abnormalities in the process of genomic imprinting on chromosome 11 lead to a loss ...
- ... Rubin MA. New strategies in prostate cancer: translating genomics into the clinic. Clin Cancer Res. 2013 Feb ... article on PubMed Central Nakagawa H. Prostate cancer genomics by high-throughput technologies: genome-wide association study ...
- ... N, Eichler EE, Bellanne-Chantelot C. Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, ... VR, Cheung SW. Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12. Eur J Hum Genet. ...
- ... gene expression are caused by a phenomenon called genomic imprinting. Both chromosome 7 and chromosome 11 contain groups of genes that normally undergo genomic imprinting; some of these genes are active only ...
- ... VR, Gibbs RA; Baylor-Hopkins Center for Mendelian Genomics; Lupski JR, Brunner HG, van Bon BW, Carvalho ... SN, Gibbs RA; Baylor-Hopkins Center for Mendelian Genomics; Brunner HG, Sutton VR, Lupski JR, Carvalho CMB. ...
- ... PubMed Central Giusti-Rodriguez P, Sullivan PF. The genomics of schizophrenia: update and implications. J Clin Invest. ... PubMed Central Schizophrenia Working Group of the Psychiatric Genomics Consortium. Biological insights from 108 schizophrenia-associated genetic ...
- ... play a role in a phenomenon known as genomic imprinting. Through genomic imprinting certain genes are turned off (inactivated) based ... mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte. Am J Hum ...