Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder-exstrophy-epispadias complex

Birth Defects Research Part A - Clinical and Molecular Teratology

Volumn 97, Issue 12, 2013, Pages 759-763

  Qi, Lihong ^a   Wang, Mei ^b   Yagnik, Garima ^a   Mattheisen, Manuel ^c   Gearhart, John P ^d   lakshmanan, Yegappan ^e   Ebert, Anne Karolin ^f   Rösch, Wolfgang ^f,g   Ludwig, Michael ^h   Draaken, Markus ^h   Reutter, Heiko ^h   Boyadjiev, Simeon A ^a,d  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c AARHUS UNIVERSITY   (Denmark)

^d JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e CHILDREN'S HOSPITAL OF MICHIGAN   (United States)

^f Barmherzige Brüder Hospital St Hedwig Regensburg   (Germany)

^g UNIVERSITY HOSPITAL REGENSBURG   (Germany)

^h UNIVERSITY OF BONN   (Germany)

Author keywords

Association study; BEEC; Bladder exstrophy; Candidate gene; Case parent trio; Epispadias; p63

Indexed keywords

PROTEIN P63;

ARTICLE; BLADDER EXSTROPHY EPISPADIAS COMPLEX; BLADDER MALFORMATION; EPISPADIAS; EUROPEAN AMERICAN; FEMALE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENOTYPE; HAPLOTYPE; HIGH THROUGHPUT SCREENING; HUMAN; MAJOR CLINICAL STUDY; MALE; MULTIPLE MALFORMATION SYNDROME; PARENT; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

ASSOCIATION STUDY; BEEC; BLADDER EXSTROPHY; CANDIDATE GENE; CASE-PARENT TRIO; EPISPADIAS; P63;

ASYMPTOMATIC DISEASES; BLADDER EXSTROPHY; EPISPADIAS; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION STUDIES; HAPLOTYPES; HIGH-THROUGHPUT NUCLEOTIDE SEQUENCING; HUMANS; INHERITANCE PATTERNS; LINKAGE DISEQUILIBRIUM; MALE; MEMBRANE PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; URINARY BLADDER;

EID: 84890425832     PISSN: 15420752     EISSN: 15420760     Source Type: Journal    
DOI: 10.1002/bdra.23161     Document Type: Article

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