Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: Report of novel pathogenic copy number variants
about
Syndromic obesity: clinical implications of a correct diagnosis.Investigation of selected genomic deletions and duplications in a cohort of 338 patients presenting with syndromic obesity by multiplex ligation-dependent probe amplification using synthetic probesTwo New Cases of 1p21.3 Deletions and an Unbalanced Translocation t(8;12) among Individuals with Syndromic Obesity.Incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1.6q16.3q23.3 duplication associated with Prader-Willi-like syndrome.Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity.Genetic analysis of very obese children with autism spectrum disorder.Chronic exposure to ethanol of male mice before mating produces attention deficit hyperactivity disorder-like phenotype along with epigenetic dysregulation of dopamine transporter expression in mouse offspring.Chromosomal microarray analysis in the genetic evaluation of 279 patients with syndromic obesity.
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P2860
Obesity with associated developmental delay and/or learning disability in patients exhibiting additional features: Report of novel pathogenic copy number variants
description
im Februar 2013 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 07 February 2013
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в лютому 2013
@uk
name
Obesity with associated develo ...... athogenic copy number variants
@en
Obesity with associated develo ...... athogenic copy number variants
@nl
type
label
Obesity with associated develo ...... athogenic copy number variants
@en
Obesity with associated develo ...... athogenic copy number variants
@nl
prefLabel
Obesity with associated develo ...... athogenic copy number variants
@en
Obesity with associated develo ...... athogenic copy number variants
@nl
P2093
P2860
P50
P356
P1476
Obesity with associated develo ...... athogenic copy number variants
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P2093
Ana Beatriz Alvarez Perez
Celia Priszkulnik Koiffmann
Charles Marques Lourenço
Cláudia Irene Emílio de Castro
Ilana Kohl
Monica Castro Varela
P2860
P304
P356
10.1002/AJMG.A.35761
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P577
2013-02-07T00:00:00Z