The Variant inv(2)(p11.2q13) Is a Genuinely Recurrent Rearrangement but Displays Some Breakpoint Heterogeneity

Human chromosome 2 contains large blocks of segmental duplications (SDs), both within and between proximal 2p and proximal 2q, and these may contribute to the frequency of the common variant inversion inv(2)(p11.2q13). Despite their being cytogenetically homogeneous, we have identified four differen...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Fickelscher, Ina , Liehr, Thomas , Watts, Kathryn , Bryant, Victoria , Barber, John C. K. , Heidemann, Simone , Siebert, Reiner , Hertz, Jens Michael , Tümer, Zeynep , Simon Thomas, N. 
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Human Genetics 2007
Assuntos:
Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2227935/
https://ncbi.nlm.nih.gov/pubmed/17847011
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados