Chrome Extension
WeChat Mini Program
Use on ChatGLM
VIPCreated with Sketch.

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,Steve Seltzsam,Bixia Zheng,Luca Schierbaum,Sophia Schneider,Nina Mann,Dervla M. Connaughton,Makiko Nakayama,Amelie T. van der Ven,Rufeng Dai,Caroline M. Kolvenbach,Franziska Kause,Isabel Ottlewski,Natasa Stajic,Neveen A. Soliman,Jameela A. Kari,Sherif El Desoky,Hanan M. Fathy,Danko Milosevic,Daniel Turudic,Muna Al Saffar,Hazem S. Awad,Loai A. Eid,Aravind Ramanathan,Prabha Senguttuvan,Shrikant M. Mane,Richard S. Lee,Stuart B. Bauer,Weining Lu,Alina C. Hilger,Velibor Tasic,Shirlee Shril,Simone Sanna-Cherchi,Friedhelm Hildebrandt

European Urology Open Science（2022）

Cited 7|Views38
Key words
Congenital anomalies of the kidney and urinary tract,Vesicoureteral reflux,Copy number variation,Whole-exome sequencing,Monogenic disease causation,Renal developmental
AI Read Science
Must-Reading Tree
Example
Generate MRT to find the research sequence of this paper
Chat Paper
Summary is being generated by the instructions you defined