Monozygotic Twins with 17q21.31 Microdeletion Syndrome

Genetic, environmental and stochastic factors in monozygotic twin discordance with a focus on epigenetic differences

(2012) Witold Czyz et al.   BMC Medicine

Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGH

(2012) M Rio et al.   CLINICAL GENETICS

Two families with sibling recurrence of the 17q21.31 microdeletion syndrome due to low-grade mosaicism

(2012) David A Koolen et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Mutations in KANSL1 cause the 17q21.31 microdeletion syndrome phenotype

(2012) Marcella Zollino et al.   NATURE GENETICS

Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome

(2012) David A Koolen et al.   NATURE GENETICS

Structural diversity and African origin of the 17q21.31 inversion polymorphism

(2012) Karyn Meltz Steinberg et al.   NATURE GENETICS

Chromosome 22q11.2 microdeletion in monozygotic twins with discordant phenotype and deletion size

(2012) Ashutosh Halder et al.   Molecular Cytogenetics

Blood Ties: Chimerism Can Mask Twin Discordance in High-Throughput Sequencing

(2011) Yaniv Erlich   Twin Research and Human Genetics

Copy number variations are not modifiers of phenotypic expression in a pair of identical twins carrying a BRCA1 mutation

(2010) A. Lasa et al.   BREAST CANCER RESEARCH AND TREATMENT

Failure to Confirm CNVs as of Aetiological Significance in Twin Pairs Discordant for Schizophrenia

(2010) Shinji Ono et al.   Twin Research and Human Genetics

DNA methylation profiles in monozygotic and dizygotic twins

(2009) Zachary A Kaminsky et al.   NATURE GENETICS

Novel microdeletion syndromes detected by chromosome microarrays

(2008) Anne M. Slavotinek   HUMAN GENETICS