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Volumn 158 A, Issue 7, 2012, Pages 1785-1787
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Contribution of LPP copy number and sequence changes to esophageal atresia, tracheoesophageal fistula, and VACTERL association
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Author keywords
[No Author keywords available]
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Indexed keywords
ALLELE;
ANORECTAL MALFORMATION;
ARTICLE;
CLINICAL ARTICLE;
DISEASE ASSOCIATION;
ESOPHAGUS ATRESIA;
EXON;
GENE;
GENE DELETION;
GENE DOSAGE;
GENE FREQUENCY;
GENE FUNCTION;
GENE SEQUENCE;
GENETIC ASSOCIATION;
GENETIC SCREENING;
HEART DISEASE;
HOMOZYGOTE;
HUMAN;
LPP GENE;
PHENOTYPE;
PRIORITY JOURNAL;
SINGLE NUCLEOTIDE POLYMORPHISM;
TRACHEOESOPHAGEAL FISTULA;
VERTEBRA MALFORMATION;
ALLELES;
ANAL CANAL;
CYTOSKELETAL PROTEINS;
ESOPHAGEAL ATRESIA;
ESOPHAGUS;
GENE DOSAGE;
GENETIC ASSOCIATION STUDIES;
HEART DEFECTS, CONGENITAL;
HUMANS;
KIDNEY;
LIM DOMAIN PROTEINS;
LIMB DEFORMITIES, CONGENITAL;
POLYMORPHISM, SINGLE NUCLEOTIDE;
SPINE;
TRACHEA;
TRACHEOESOPHAGEAL FISTULA;
FISTULA;
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EID: 84862650486
PISSN: 15524825
EISSN: 15524833
Source Type: Journal
DOI: 10.1002/ajmg.a.35391 Document Type: Article |
Times cited : (10)
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References (6)
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