De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus.
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Novel IRF6 mutations in families with Van Der Woude syndrome and popliteal pterygium syndrome from sub-Saharan AfricaA genome-wide study of inherited deletions identified two regions associated with nonsyndromic isolated oral clefts.Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex.Challenges in non-invasive prenatal screening for sub-chromosomal copy number variations using cell-free DNA.Genome-wide copy number scan identifies IRF6 involvement in Van der Woude syndrome in an Indian family.A Novel Interferon Regulatory Factor 6 Mutation in an Asian Family With Van der Woude Syndrome.Application of high resolution SNP arrays in patients with congenital oral clefts in south China.
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De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 06 August 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus.
@en
De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus.
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type
label
De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus.
@en
De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus.
@nl
prefLabel
De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus.
@en
De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus.
@nl
P2093
P2860
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P1476
De novo 2.3 Mb microdeletion of 1q32.2 involving the Van der Woude Syndrome locus.
@en
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Eileen Cp Lim
Ene-Choo Tan
Seng-Teik Lee
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P2888
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10.1186/1755-8166-6-31
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2013-08-06T00:00:00Z
P5875
P6179
1025554563