De novo deletions and duplications detected by array CGH: a study of parental origin in relation to mechanisms of formation and size of imbalance

Mechanisms for Nonrecurrent Genomic Rearrangements Associated with CMT1A or HNPP: Rare CNVs as a Cause for Missing Heritability

(2010) Feng Zhang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Advanced age increases chromosome structural abnormalities in human spermatozoa

(2010) Cristina Templado et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

De novo rates and selection of large copy number variation

(2010) A. Itsara et al.   GENOME RESEARCH

Cryptic genomic imbalances in de novo and inherited apparently balanced chromosomal rearrangements: Array CGH study of 47 unrelated cases

(2009) Caroline Schluth-Bolard et al.   European Journal of Medical Genetics

Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture

(2009) Lisenka E.L.M. Vissers et al.   HUMAN MOLECULAR GENETICS

De novo apparently balanced translocations in man are predominantly paternal in origin and associated with a significant increase in paternal age

(2009) N. S. Thomas et al.   JOURNAL OF MEDICAL GENETICS

A Microhomology-Mediated Break-Induced Replication Model for the Origin of Human Copy Number Variation

(2009) P. J. Hastings et al.   PLoS Genetics

Breakpoint Mapping and Array CGH in Translocations: Comparison of a Phenotypically Normal and an Abnormal Cohort

(2008) Julia Baptista et al.   AMERICAN JOURNAL OF HUMAN GENETICS