Mutational analyses of UPIIIA, SHH, EFNB2, and HNF1β in persistent cloaca and associated kidney malformations-Reference-Cited by-同舟云学术

Mutational analyses of UPIIIA, SHH, EFNB2, and HNF1β in persistent cloaca and associated kidney malformations

Published:2007-02 Issue:1 Volume:3 Page:2-9
ISSN:1477-5131
Container-title:Journal of Pediatric Urology
language:en
Short-container-title:Journal of Pediatric Urology

Author:

Jenkins Dagan,Bitner-Glindzicz Maria,Thomasson Louise,Malcolm Sue,Warne Stephanie A.,Feather Sally A.,Flanagan Sarah E.,Ellard Sian,Bingham Coralie,Santos Lane,Henkemeyer Mark,Zinn Andrew,Baker Linda A.,Wilcox Duncan T.,Woolf Adrian S.

Publisher

Elsevier BV

Subject

Urology,Pediatrics, Perinatology and Child Health

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3. Long-term urological outcome in patients presenting with persistent cloaca;Warne;J Urol,2002

4. Long-term gynecological outcome of patients with persistent cloaca;Warne;J Urol,2003

5. Surgical reconstruction of cloacal malformations can alter bladder function: a comparative study with anorectal anomalies;Warne;J Urol,2004

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1. Molecular biology, genetic, and epigenetics female urology;Genetics and Epigenetics of Genitourinary Diseases;2025

2. A novel genotype-phenotype between persistent-cloaca-related VACTERL and mutations of 8p23 and 12q23.1;Pediatric Research;2023-12-22

3. A Review of Diagnosis and Management: Persistent Cloaca Treated by a Posterior Sagittal Approach With a Normal Functional Outcome;Cureus;2022-04-01

4. EFNB2haploinsufficiency causes a syndromic neurodevelopmental disorder;Clinical Genetics;2018-03-15

5. De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca;Human Molecular Genetics;2017-11-21