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Gabriel C Dworschak

Showing results (1-10 of 31) with videos related to

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Orphanet Journal of Rare Diseases|April 10, 2021
Currarino syndrome: a comprehensive genetic review of a rare congenital disorderGabriel C Dworschak, Heiko M Reutter, Michael Ludwig
Annals of Translational Medicine|December 7, 2019
Expanding the knowledge on development of CAKUT: molecular genetics and beyondGabriel C Dworschak, Heiko Reutter, Alina C Hilger
Pediatric Nephrology (Berlin, Germany)|January 9, 2014
Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humansAsaf Vivante, Stefan Kohl, Daw-Yang Hwang, et al.
Genes|September 28, 2021
The Role of De Novo Variants in Formation of Human Anorectal MalformationsGabriel C Dworschak, Iris A L M van Rooij, Heiko M Reutter
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 14, 2015
Increased psychosocial risk, depression and reduced quality of life living with autosomal dominant polycystic kidney diseaseRoslyn J Simms, Kah Mean Thong, Gabriel C Dworschak, et al.
International Journal of Molecular Medicine|May 15, 2013
An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndromeGabriel C Dworschak, Markus Draaken, Alina Hilger, et al.
Frontiers in Pediatrics|June 21, 2018
<i>De Novo</i> Duplication of 11p15 Associated With Congenital Diaphragmatic HerniaGabriel C Dworschak, Hartmut Engels, Jessica Becker, et al.
Molecular and Cellular Pediatrics|March 28, 2023
Modelling human lower urinary tract malformations in zebrafishCaroline M Kolvenbach, Gabriel C Dworschak, Johanna M Rieke, et al.
Orphanet Journal of Rare Diseases|December 15, 2017
Epidemiologic analysis of families with isolated anorectal malformations suggests high prevalence of autosomal dominant inheritanceGabriel C Dworschak, Nadine Zwink, Eberhard Schmiedeke, et al.
Journal of the American Society of Nephrology : JASN|April 5, 2014
Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tractStefan Kohl, Daw-Yang Hwang, Gabriel C Dworschak, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Orphanet Journal of Rare Diseases|April 10, 2021
Currarino syndrome: a comprehensive genetic review of a rare congenital disorderGabriel C Dworschak, Heiko M Reutter, Michael Ludwig
Annals of Translational Medicine|December 7, 2019
Expanding the knowledge on development of CAKUT: molecular genetics and beyondGabriel C Dworschak, Heiko Reutter, Alina C Hilger
Pediatric Nephrology (Berlin, Germany)|January 9, 2014
Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humansAsaf Vivante, Stefan Kohl, Daw-Yang Hwang, et al.
Genes|September 28, 2021
The Role of De Novo Variants in Formation of Human Anorectal MalformationsGabriel C Dworschak, Iris A L M van Rooij, Heiko M Reutter
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 14, 2015
Increased psychosocial risk, depression and reduced quality of life living with autosomal dominant polycystic kidney diseaseRoslyn J Simms, Kah Mean Thong, Gabriel C Dworschak, et al.
International Journal of Molecular Medicine|May 15, 2013
An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndromeGabriel C Dworschak, Markus Draaken, Alina Hilger, et al.
Frontiers in Pediatrics|June 21, 2018
<i>De Novo</i> Duplication of 11p15 Associated With Congenital Diaphragmatic HerniaGabriel C Dworschak, Hartmut Engels, Jessica Becker, et al.
Molecular and Cellular Pediatrics|March 28, 2023
Modelling human lower urinary tract malformations in zebrafishCaroline M Kolvenbach, Gabriel C Dworschak, Johanna M Rieke, et al.
Orphanet Journal of Rare Diseases|December 15, 2017
Epidemiologic analysis of families with isolated anorectal malformations suggests high prevalence of autosomal dominant inheritanceGabriel C Dworschak, Nadine Zwink, Eberhard Schmiedeke, et al.
Journal of the American Society of Nephrology : JASN|April 5, 2014
Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tractStefan Kohl, Daw-Yang Hwang, Gabriel C Dworschak, et al.
Pageof 4