Deciphering the mutation spectrum in south Indian children with congenital anomalies of the kidney and urinary tract | BMC Nephrology | Full Text
Whole-Exome Sequencing Identifies Causative Mutations in Families with Congenital Anomalies of the Kidney and Urinary Tract. - Abstract - Europe PMC
Molecular diagnostic in fetuses with isolated congenital anomalies of the kidney and urinary tract by whole‐exome sequencing - Zhou - 2020 - Journal of Clinical Laboratory Analysis - Wiley Online Library
Genes | Free Full-Text | Missense Variants in GFRA1 and NPNT Are Associated with Congenital Anomalies of the Kidney and Urinary Tract
CAKUT Manejo antenatal y postnatal. Opiniones actuales – Dr. Germán Falke (Argentina) | Asociación Latinoamericana de Nefrología Pediátrica – ALANEPE
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An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease | npj Genomic Medicine
Exome Sequencing and Identification of Phenocopies in Patients With Clinically Presumed Hereditary Nephropathies - American Journal of Kidney Diseases
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A homozygous missense variant in VWA2, encoding an interactor of the Fraser-complex, in a patient with vesicoureteral reflux | PLOS ONE
Prenatal Genetic Considerations of Congenital Anomalies of The Kidney and Urinary Tract (CAKUT) | PDF | Genetic Disorder | Kidney
Genetics of Congenital Anomalies of the Kidneys and Urinary Tract | SpringerLink
Recessive mutations in CAKUT and VACTERL association - ScienceDirect
Challenges in genetic counseling for congenital anomalies of the kidneys and urinary tract (CAKUT) spectrum
Síndromes Hereditarios con Afectación Renal | Nefrología al día
Genes investigated in unrelated patients with isolated congenital... | Download Table
JCM | Free Full-Text | Targeted Exome Sequencing Provided Comprehensive Genetic Diagnosis of Congenital Anomalies of the Kidney and Urinary Tract
Summary of RET pathway mutations in CAKUT studies | Download Table
Invitae - Invitae Congenital Anomalies of Kidney and Urinary Tract (CAKUT) Panel - Clinical Description - Page 1
Spotlight on Genetic Kidney Diseases: A Call for Drug Delivery and Nanomedicine Solutions | ACS Nano
Challenges in genetic counseling for congenital anomalies of the kidneys and urinary tract (CAKUT) spectrum
![PDF] Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT). | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/9f4ce66772e6186bbdcaa2b226d1d6be8c9399eb/4-Table2-1.png "PDF] Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT). | Semantic Scholar")
PDF] Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT). | Semantic Scholar
Prioritization and burden analysis of rare variants in 208 candidate genes suggest they do not play a major role in CAKUT
Impact of next generation sequencing on our understanding of CAKUT - ScienceDirect
Genetic, environmental, and epigenetic factors involved in CAKUT | Nature Reviews Nephrology
