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Pediatric Nephrology (Berlin, Germany)
|
September 7, 2002
Nail-patella syndrome. Overview on clinical and molecular findings
Ernie M H F Bongers, Marie-Claire Gubler, Nine V A M Knoers
Knee Surgery, Sports Traumatology, Arthroscopy : Official Journal of the ESSKA
|
January 6, 2006
Minimal rotation aberrations cause radiographic misdiagnosis of trochlear dysplasia
Sander Koëter, Ernie M H F Bongers, Jacky de Rooij, et al.
European Journal of Medical Genetics
|
February 8, 2021
Polycystic liver disease genes: Practical considerations for genetic testing
Melissa M Boerrigter, Ernie M H F Bongers, Dorien Lugtenberg, et al.
Nature Reviews. Nephrology
|
August 19, 2015
Genetic, environmental, and epigenetic factors involved in CAKUT
Nayia Nicolaou, Kirsten Y Renkema, Ernie M H F Bongers, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
September 23, 2018
Nephrotic Syndrome With Mutations in NPHS2: The Role of R229Q and Implications for Genetic Counseling
Ilse M Rood, Jeroen K J Deegens, Dorien Lugtenberg, et al.
International Journal of Molecular Medicine
|
June 7, 2003
Confirmation of CLIM2/LMX1B interaction by yeast two-hybrid screening and analysis of its involvement in nail-patella syndrome
Monica Marini, Ernie M H F Bongers, Roberto Cusano, et al.
Plos Genetics
|
March 22, 2013
Deficiency in origin licensing proteins impairs cilia formation: implications for the aetiology of Meier-Gorlin syndrome
Tom Stiff, Meryem Alagoz, Diana Alcantara, et al.
Nephron
|
December 23, 2014
Functional models for congenital anomalies of the kidney and urinary tract
Glenn van de Hoek, Nayia Nicolaou, Rachel H Giles, et al.
American Journal of Medical Genetics. Part A
|
March 18, 2009
Xq13.2q21.1 duplication encompassing the ATRX gene in a man with mental retardation, minor facial and genital anomalies, short stature and broad thorax
Dorien Lugtenberg, Arjan P M de Brouwer, Astrid R Oudakker, et al.
Journal of the American Society of Nephrology : JASN
|
August 31, 2000
Nail-patella syndrome: identification of mutations in the LMX1B gene in Dutch families
Nine V A M Knoers, Ernie M H F Bongers, Sylvia E C VAN Beersum, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 64) with videos related to
Sort By:
Page
of 7
Pediatric Nephrology (Berlin, Germany)
|
September 7, 2002
Nail-patella syndrome. Overview on clinical and molecular findings
Ernie M H F Bongers, Marie-Claire Gubler, Nine V A M Knoers
Knee Surgery, Sports Traumatology, Arthroscopy : Official Journal of the ESSKA
|
January 6, 2006
Minimal rotation aberrations cause radiographic misdiagnosis of trochlear dysplasia
Sander Koëter, Ernie M H F Bongers, Jacky de Rooij, et al.
European Journal of Medical Genetics
|
February 8, 2021
Polycystic liver disease genes: Practical considerations for genetic testing
Melissa M Boerrigter, Ernie M H F Bongers, Dorien Lugtenberg, et al.
Nature Reviews. Nephrology
|
August 19, 2015
Genetic, environmental, and epigenetic factors involved in CAKUT
Nayia Nicolaou, Kirsten Y Renkema, Ernie M H F Bongers, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
September 23, 2018
Nephrotic Syndrome With Mutations in NPHS2: The Role of R229Q and Implications for Genetic Counseling
Ilse M Rood, Jeroen K J Deegens, Dorien Lugtenberg, et al.
International Journal of Molecular Medicine
|
June 7, 2003
Confirmation of CLIM2/LMX1B interaction by yeast two-hybrid screening and analysis of its involvement in nail-patella syndrome
Monica Marini, Ernie M H F Bongers, Roberto Cusano, et al.
Plos Genetics
|
March 22, 2013
Deficiency in origin licensing proteins impairs cilia formation: implications for the aetiology of Meier-Gorlin syndrome
Tom Stiff, Meryem Alagoz, Diana Alcantara, et al.
Nephron
|
December 23, 2014
Functional models for congenital anomalies of the kidney and urinary tract
Glenn van de Hoek, Nayia Nicolaou, Rachel H Giles, et al.
American Journal of Medical Genetics. Part A
|
March 18, 2009
Xq13.2q21.1 duplication encompassing the ATRX gene in a man with mental retardation, minor facial and genital anomalies, short stature and broad thorax
Dorien Lugtenberg, Arjan P M de Brouwer, Astrid R Oudakker, et al.
Journal of the American Society of Nephrology : JASN
|
August 31, 2000
Nail-patella syndrome: identification of mutations in the LMX1B gene in Dutch families
Nine V A M Knoers, Ernie M H F Bongers, Sylvia E C VAN Beersum, et al.
Page
of 7