Related references
Note: Only part of the references are listed.Clinical and molecular delineation of 16p13.3 duplication in a patient with congenital heart defect and multiple congenital anomalies
Jin-Lan Chen et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2012)
Phenotypic manifestations of copy number variation in chromosome 16p13.11
Sandesh C. Sreenath Nagamani et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2011)
Copy number variations of chromosome 16p13.1 region associated with schizophrenia
A. Ingason et al.
MOLECULAR PSYCHIATRY (2011)
Extending the Phenotype of Monosomy 1p36 Syndrome and Mapping of a Critical Region for Obesity and Hyperphagia
Carla S. D'Angelo et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2010)
Refinement of Causative Genes in Monosomy 1p36 Through Clinical and Molecular Cytogenetic Characterization of Small Interstitial Deletions
Jill A. Rosenfeld et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2010)
High-resolution SNP arrays in mental retardation diagnostics: how much do we gain?
Laura Bernardini et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2010)
The paternal effect of chromosome translocation carriers observed from meiotic segregation in embryos
Belen Lledo et al.
HUMAN REPRODUCTION (2010)
Duplications of the critical Rubinstein-Taybi deletion region on chromosome 16p13.3 cause a novel recognisable syndrome
Bernard Thienpont et al.
JOURNAL OF MEDICAL GENETICS (2010)
Clinical Genetic Testing for Patients With Autism Spectrum Disorders
Yiping Shen et al.
PEDIATRICS (2010)
Idiopathic mental retardation and new chromosomal abnormalities
Cinzia Galasso et al.
ITALIAN JOURNAL OF PEDIATRICS (2010)
16p subtelomeric duplication: a clinically recognizable syndrome
Maria Cristina Digilio et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2009)
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant
F. D. Hannes et al.
JOURNAL OF MEDICAL GENETICS (2009)
Duplication of the Rubinstein-Taybi region on 16p13.3 is associated with a distinctive phenotype
Giuseppe Marangi et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2008)
Further delineation of deletion 1p36 syndrome in 60 patients: A recognizable phenotype and common cause of developmental delay and mental retardation
Agatino Battaglia et al.
PEDIATRICS (2008)
Monosomy 1p36 deletion syndrome
Marzena Gajecka et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS (2007)
Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation
Reinhard Ullmann et al.
HUMAN MUTATION (2007)
Trisomy 16p: A longitudinal profile and photo essay
A Sommer et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)
Human subtelomere structure and variation
H Riethman et al.
CHROMOSOME RESEARCH (2005)
Population data suggest that deletions of 1p36 are a relatively common chromosome abnormality
HA Heilstedt et al.
CLINICAL GENETICS (2003)
The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation
J Flint et al.
CURRENT OPINION IN GENETICS & DEVELOPMENT (2003)
Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome
HA Heilstedt et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2003)
Meiotic outcomes in reciprocal translocation carriers ascertained in 3-day human embryos
CM Ogilvie et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2002)
Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3)
E Holinski-Feder et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)