Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation.
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Haploinsufficiency of TAB2 causes congenital heart defects in humansCleft lip and palate: understanding genetic and environmental influencesPrevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndromeGenomic expression in non syndromic cleft lip and palate patients: A reviewCleft lip - a comprehensive reviewNew insights into craniofacial malformationsENDEAVOUR update: a web resource for gene prioritization in multiple speciesA genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate riskA male with unilateral microphthalmia reveals a role for TMX3 in eye developmentCleft lip and palate genetics and application in early embryological development.Chromosomal abnormalities among children born with conotruncal cardiac defects.A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients.Search for genomic alterations in monozygotic twins discordant for cleft lip and/or palateHaploinsufficiency of insulin gene enhancer protein 1 (ISL1) is associated with d-transposition of the great arteries.A combined targeted mutation analysis of IRF6 gene would be useful in the first screening of oral facial clefts.Developmental microRNA expression profiling of murine embryonic orofacial tissue.Identification of functional variants for cleft lip with or without cleft palate in or near PAX7, FGFR2, and NOG by targeted sequencing of GWAS loci.A genome-wide study of inherited deletions identified two regions associated with nonsyndromic isolated oral clefts.Risk of breast cancer in families with cleft lip and palate.Discovery of candidate genes for nonsyndromic cleft lip palate through genome-wide linkage analysis of large extended families in the Malay population.Genetics of nonsyndromic orofacial cleftsClinical Aspects associated with Syndromic forms of Orofacial Clefts in a Colombian population.Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex.Copy number variation analysis identifies novel CAKUT candidate genes in children with a solitary functioning kidney.De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus.SCRIB and PUF60 are primary drivers of the multisystemic phenotypes of the 8q24.3 copy-number variant.Current concepts in genetics of nonsyndromic cleftsGenetics of cleft lip and cleft palate.An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects.Diazepam effects on non-syndromic cleft lip with or without palate: epidemiological studies, clinical findings, genes and extracellular matrix.Prenatal diagnosis by array-comparative genomic hybridization.Genetic architecture of reciprocal CNVs.Genomic approaches for studying craniofacial disorders.Gene expression profiling analysis contributes to understanding the association between non-syndromic cleft lip and palate, and cancer.Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play.Renal agenesis in Kallmann syndrome: a network approach.Tbx1 regulates oral epithelial adhesion and palatal development.Predictor(s) of Abnormal Array Comparative Genomic Hybridization Results in Patients With Cleft Lip and/or Palate.Genetic basis of human congenital anomalies of the kidney and urinary tract.Identification of Isthmin 1 as a Novel Clefting and Craniofacial Patterning Gene in Humans.
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P2860
Identification of novel candidate genes associated with cleft lip and palate using array comparative genomic hybridisation.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 14 September 2007
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
@cs
name
Identification of novel candid ...... arative genomic hybridisation.
@en
Identification of novel candid ...... arative genomic hybridisation.
@nl
type
label
Identification of novel candid ...... arative genomic hybridisation.
@en
Identification of novel candid ...... arative genomic hybridisation.
@nl
prefLabel
Identification of novel candid ...... arative genomic hybridisation.
@en
Identification of novel candid ...... arative genomic hybridisation.
@nl
P2093
P2860
P356
P1476
Identification of novel candid ...... arative genomic hybridisation.
@en
P2093
A C Lidral
B C Schutte
E F P M Schoenmakers
E J Lammer
G M Vessere
J C Murray
J L'Heureux
P2860
P356
10.1136/JMG.2007.052191
P407
P577
2007-09-14T00:00:00Z