A homozygousHOXA11variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract-Reference-Cited by-同舟云学术

A homozygousHOXA11variation as a potential novel cause of autosomal recessive congenital anomalies of the kidney and urinary tract

Author:

Saygili Seha¹^ORCID,Atayar Emine²,Canpolat Nur¹,Elicevik Mehmet³,Kurugoglu Sebuh⁴,Sever Lale¹,Caliskan Salim¹,Ozaltin Fatih²⁵^ORCID

Affiliation:

1. Department of Pediatric Nephrology Istanbul University‐Cerrahpasa, Cerrahpasa Faculty of Medicine Istanbul Turkey

2. Nephrogenetics Laboratory, Department of Pediatric Nephrology Hacettepe University Faculty of Medicine Ankara Turkey

3. Department of Pediatric Surgery Istanbul University‐Cerrahpasa, Cerrahpasa Faculty of Medicine Istanbul Turkey

4. Department of Pediatric Radiology Istanbul University‐Cerrahpasa, Cerrahpasa Faculty of Medicine Istanbul Turkey

5. Department of Pediatric Nephrology Hacettepe University Faculty of Medicine Ankara Turkey

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference24 articles.

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