Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genome-wide linkage scan for bladder exstrophy-epispadias complex.

Birth defects research. Part A, Clinical and molecular teratology - 1 Feb 2009

Ludwig Michael, Rüschendorf Franz, Saar Kathrin, Hübner Norbert, Siekmann Lothar, Boyadjiev Simeon A, Reutter Heiko

Abstract excerpt

BACKGROUND: The bladder exstrophy-epispadias complex represents a spectrum of urogenital anomalies in which part or all of the distal urinary tract fail to close and are exposed on the outer abdominal wall. Previous studies are suggestive of an underlying multifactorial mode of inheritance. Howev...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Abnormalities, Multiple
Share to Chromosome Mapping
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome-Wide Association Study

Share to Genotype

Share to Lod Score

Share to Pedigree

Share to Polymorphism, Single Nucleotide

Source

Identifiers

PMID: 19086019
DOI: 10.1002/bdra.20512

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19086019-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genome-wide linkage scan for bladder exstrophy-epispadias complex.PMID 19086019Read ↗

Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family.Semantic proximity Read ↗

Epidemiological survey of 214 families with bladder exstrophy-epispadias complex.Semantic proximity Read ↗

Genetics of Bladder-Exstrophy-Epispadias Complex (BEEC): Systematic Elucidation of Mendelian and Multifactorial PhenotypesSemantic proximity Read ↗

Clinical and molecular characterization of the bladder exstrophy‐epispadias complex: analysis of 232 familiesSemantic proximity Read ↗

The Genomic Architecture of Bladder Exstrophy Epispadias Complex.Semantic proximity Read ↗

Genome-wide Association Study and Meta-Analysis Identify ISL1 as Genome-wide Significant Susceptibility Gene for Bladder ExstrophySemantic proximity Read ↗

Phenotype severity in the bladder exstrophy-epispadias complex: analysis of genetic and nongenetic contributing factors in 441 families from North America and Europe.Semantic proximity Read ↗

Genome-wide association study and mouse expression data identify a highly conserved 32 kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder.Semantic proximity Read ↗

New Insights on the Basic Science of Bladder Exstrophy-epispadias Complex.Semantic proximity Read ↗

Candidate gene association study implicates p63 in the etiology of nonsyndromic bladder-exstrophy-epispadias complex.Semantic proximity Read ↗

Seven new cases of familial isolated bladder exstrophy and epispadias complex (BEEC) and review of the literatureSemantic proximity Read ↗

Genome-wide linkage analysis for hypospadias susceptibility genes.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.