Copy number variants suggest different molecular pathways for the pathogenesis of bladder exstrophy-Reference-Cited by-同舟云学术

Copy number variants suggest different molecular pathways for the pathogenesis of bladder exstrophy

Published:2022-11-08 Issue:2 Volume:191 Page:378-390
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:American J of Med Genetics Pt A

Author:

Nordenskjöld Agneta¹²^ORCID,Arkani Samara¹³,Pettersson Maria⁴⁵^ORCID,Winberg Johanna⁴⁵^ORCID,Cao Jia¹,Fossum Magdalena¹⁶,Anderberg Magnus⁷⁸,Barker Gillian⁹,Holmdahl Gundela¹²¹⁰¹¹,Lundin Johanna⁴⁵

Affiliation:

1. Department of Women's and Children's Health, and Center for Molecular Medicine Karolinska Institutet Stockholm Sweden

2. Pediatric Surgery Astrid Lindgren Children Hospital, Karolinska University Hospital Stockholm Sweden

3. Department of Urology Danderyds Hospital Danderyd Sweden

4. Department of Clinical Genetics Karolinska University Hospital Stockholm Sweden

5. Department of Molecular Medicine and Surgery Karolinska Institutet Stockholm Sweden

6. Department of Pediatric Surgery Copenhagen University, Righospitalet København Denmark

7. Department of Pediatric Surgery Skåne University Hospital Lund Sweden

8. Department of Clinical Sciences Lund University Lund Sweden

9. Department of Pediatric Surgery Uppsala Academic Hospital Uppsala Sweden

10. Sahlgrenska Academy Women's and Children's Health Gothenburg Sweden

11. Department of Pediatric Surgery Queen Silvia's Children's Hospital Gothenburg Sweden

Funder

Vetenskapsrådet

Kommunfullmäktige, Stockholms Stad

Karolinska Institutet

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.63031

Reference71 articles.

1. Evaluation of the ISL1 gene in the pathogenesis of bladder exstrophy in a Swedish cohort

2. WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish

3. Wolf-Hirschhorn syndrome: A review and update

4. Update on the clinical features and natural history of Wolf-Hirschhorn (4p-) syndrome: Experience with 87 patients and recommendations for routine health supervision

5. Identification and Characterization of the Human Homologue of SH3BP2, an SH3 Binding Domain Protein within a Common Region of Deletion at 4p16.3 Involved in Bladder Cancer

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