✦ LIBER ✦

Copy Number Changes of CNV Regions in Intersubspecific Crosses of the House Mouse

✍ Scribed by Scavetta, R. J.; Tautz, D.

Book ID: 118736631
Publisher: Oxford University Press
Year: 2010
Tongue: English
Weight: 437 KB
Volume: 27
Category: Article
ISSN: 0737-4038
DOI: 10.1093/molbev/msq064

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Technical considerations for genotyping

Technical considerations for genotyping multi-allelic copy number variation (CNV), in regions of segmental duplication

✍ Cantsilieris, Stuart; Western, Patrick S; Baird, Paul N; White, Stefan J 📂 Article 📅 2014 🏛 BioMed Central 🌐 English ⚖ 242 KB

High frequency of copy number variations

High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith–Wiedemann syndrome

✍ Baskin, Berivan; Choufani, Sanaa; Chen, Yi-an; Shuman, Cheryl; Parkinson, Nicole 📂 Article 📅 2013 🏛 Springer 🌐 English ⚖ 470 KB

Characterization of copy number-stable r

Characterization of copy number-stable regions in the human genome

✍ Anna C.V. Johansson; Lars Feuk 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 292 KB

In the past few years the number of copy number variants (CNVs) identified in the human genome has increased significantly, but our understanding of the functional impact of CNVs is still limited. Clinically significant variations cannot easily be distinguished from benign, complicating interpretati

Copy number variation (CNVs) of genomic

Copy number variation (CNVs) of genomic sequences and their involvement in the development of endometriosis

✍ Mafra, F.; Amaro, A.; Pelegrino, R.; Bianco, B.; Barbosa, C.; Christofolini, D. 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 48 KB

Analysis of copy number variation (CNV)

Analysis of copy number variation (CNV) of the SPANXA-E gene family in infertile and fertile men

✍ S. Hansen; E.E. Eichler; S.M. Fullerton; B.R. Emery; D.T. Carrell 📂 Article 📅 2008 🏛 Elsevier Science 🌐 English ⚖ 62 KB

Genome-wide survey implicates the influe

Genome-wide survey implicates the influence of copy number variants (CNVs) in the development of early-onset bipolar disorder

✍ Priebe, L; Degenhardt, F A; Herms, S; Haenisch, B; Mattheisen, M; Nieratschker, 📂 Article 📅 2011 🏛 Nature Publishing Group 🌐 English ⚖ 483 KB