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The Journal of Urology
|
May 3, 2024
Expert Consensus on Pediatric Urodynamics Reporting Using Modified Delphi Technique
Kristen M Meier, Claudia Mata, Jill L Kaar, et al.
European Urology Open Science
|
October 3, 2022
Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract
Chen-Han Wilfred Wu, Tze Y Lim, Chunyan Wang, et al.
Radiology
|
September 13, 2022
Myocardial Fibrosis at Cardiac MRI Helps Predict Adverse Clinical Outcome in Patients with Mitral Valve Prolapse
Stefano Figliozzi, Georgios Georgiopoulos, Pedro M Lopes, et al.
American Journal of Human Genetics
|
August 4, 2015
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development
Asaf Vivante, Marc-Jens Kleppa, Julian Schulz, et al.
Radiology. Cardiothoracic Imaging
|
June 20, 2024
Arrhythmic Mitral Valve Prolapse Phenotype: An Unsupervised Machine Learning Analysis Using a Multicenter Cardiac MRI Registry
Ralph Kwame Akyea, Stefano Figliozzi, Pedro M Lopes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT
Steve Seltzsam, Chunyan Wang, Bixia Zheng, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 14, 2025
Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families
Lea Maria Merz, Caroline M Kolvenbach, Chunyan Wang, et al.
Journal of the American Society of Nephrology : JASN
|
August 26, 2018
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract
Amelie T van der Ven, Dervla M Connaughton, Hadas Ityel, et al.
American Journal of Human Genetics
|
September 6, 2020
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations
Dervla M Connaughton, Rufeng Dai, Danielle J Owen, et al.
Science (New York, N.Y.)
|
October 17, 2015
The Pluto system: Initial results from its exploration by New Horizons
S A Stern, F Bagenal, K Ennico, et al.
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of 65
Search research articles
Search
Showing results (641-650 of 650) with videos related to
Sort By:
Page
of 65
You have reached the last page of results.
This site can display upto 650 results.
The Journal of Urology
|
May 3, 2024
Expert Consensus on Pediatric Urodynamics Reporting Using Modified Delphi Technique
Kristen M Meier, Claudia Mata, Jill L Kaar, et al.
European Urology Open Science
|
October 3, 2022
Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract
Chen-Han Wilfred Wu, Tze Y Lim, Chunyan Wang, et al.
Radiology
|
September 13, 2022
Myocardial Fibrosis at Cardiac MRI Helps Predict Adverse Clinical Outcome in Patients with Mitral Valve Prolapse
Stefano Figliozzi, Georgios Georgiopoulos, Pedro M Lopes, et al.
American Journal of Human Genetics
|
August 4, 2015
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development
Asaf Vivante, Marc-Jens Kleppa, Julian Schulz, et al.
Radiology. Cardiothoracic Imaging
|
June 20, 2024
Arrhythmic Mitral Valve Prolapse Phenotype: An Unsupervised Machine Learning Analysis Using a Multicenter Cardiac MRI Registry
Ralph Kwame Akyea, Stefano Figliozzi, Pedro M Lopes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
Reverse phenotyping facilitates disease allele calling in exome sequencing of patients with CAKUT
Steve Seltzsam, Chunyan Wang, Bixia Zheng, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 14, 2025
Trio exome sequencing identifies de novo variants in novel candidate genes in 19.62% of CAKUT families
Lea Maria Merz, Caroline M Kolvenbach, Chunyan Wang, et al.
Journal of the American Society of Nephrology : JASN
|
August 26, 2018
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract
Amelie T van der Ven, Dervla M Connaughton, Hadas Ityel, et al.
American Journal of Human Genetics
|
September 6, 2020
Mutations of the Transcriptional Corepressor ZMYM2 Cause Syndromic Urinary Tract Malformations
Dervla M Connaughton, Rufeng Dai, Danielle J Owen, et al.
Science (New York, N.Y.)
|
October 17, 2015
The Pluto system: Initial results from its exploration by New Horizons
S A Stern, F Bagenal, K Ennico, et al.
Page
of 65