Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele.
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Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases.A genome-wide association study of copy number variations with umbilical hernia in swine.Genome-wide association study reveals a QTL and strong candidate genes for umbilical hernia in pigs on SSC14.
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Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele.
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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 April 2012
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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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Genome-wide linkage and copy n ...... utosomal dominant omphalocele.
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Genome-wide linkage and copy n ...... utosomal dominant omphalocele.
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type
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Genome-wide linkage and copy n ...... utosomal dominant omphalocele.
@en
Genome-wide linkage and copy n ...... utosomal dominant omphalocele.
@nl
prefLabel
Genome-wide linkage and copy n ...... utosomal dominant omphalocele.
@en
Genome-wide linkage and copy n ...... utosomal dominant omphalocele.
@nl
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Genome-wide linkage and copy n ...... utosomal dominant omphalocele.
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Amit K Maiti
Andrew J Sharp
Charles E Schwartz
David B Everman
Frédérique Béna
Heather L Newkirk
Jeffrey C Murray
Ken McElreavey
Maryline Gagnebin
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P304
P356
10.1136/JMEDGENET-2012-100826
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P577
2012-04-01T00:00:00Z