Mutations in DSTYK and Dominant Urinary Tract Malformations (original) (raw)

KRAS mutation is present in a small subset of primary urinary bladder adenocarcinomas

Leticia Miravalle

Histopathology, 2012

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Risk Assessment of Severe Congenital Anomalies of the Kidney and Urinary Tract (CAKUT): A Birth Cohort

Marissa Defreitas

Frontiers in Pediatrics, 2019

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De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations

Ann Nordgren

The American Journal of Human Genetics, 2016

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Mapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24

Hassan Chaib

Nephrology Dialysis Transplantation, 2009

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Multiple Genitourinary Malformations Associated with Malformations of Other Organs – As a Rarity of Case Report

masum rahman

Journal of Surgery and Research

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Syndrome in question

Aristoteles Rosmaninho

Anais Brasileiros de Dermatologia, 2016

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Implication ofFOXD2dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

Nur Canpolat

medRxiv (Cold Spring Harbor Laboratory), 2023

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Inherited partial X chromosome duplication in a mentally retarded male

Karen Brøndum-nielsen

Journal of Medical Genetics, 1982

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Mutant CHUK and Severe Fetal Encasement Malformation

Jonna Tallila

New England Journal of Medicine, 2010

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Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants

Salmo Raskin

New England Journal of Medicine, 2012

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Congenital abnormalities of the urogenital tract in association with congenital vertebral malformations

Grahame Smith

The Journal of Bone and Joint Surgery, 2002

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Asymptomatic Urinary Abnormalities

Ziauddin Ahmed

Medical Clinics of North America, 1997

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Mutations in a novel gene lead to kidney tumors, lung wall defects, and benign tumors of the hair follicle in patients with the Birt-Hogg-Dubé syndrome

Maria Merino

Cancer Cell, 2002

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Isolated Congenital Anosmia and CNGA2 Mutation

Masoud Garshasbi

Scientific Reports, 2017

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Female pelvic congenital malformations

rosa laterza

European Journal of Obstetrics & Gynecology and Reproductive Biology, 2011

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CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT)

Maria Joannou

Nephrology Dialysis Transplantation, 2011

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Molecular genetics of Dravet syndrome

Sarah Weckhuysen

Developmental Medicine & Child Neurology, 2011

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Central European Journal of Urology

George Kasyan

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A 46,XY Female DSD Patient with Bilateral Gonadoblastoma, a Novel SRY Missense Mutation Combined with a WT1 KTS Splice-Site Mutation

Remko Hersmus

PLoS ONE, 2012

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A comprehensive analysis of normal variation and disease-causing mutations in the human DSPP gene

James Hartsfield

Human Mutation, 2008

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Five Genetic Variants Associated with Prostate Cancer

Wayne Hall

New England Journal of Medicine, 2008

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Genetics and development of neural tube defects

Nicholas Greene

The Journal of Pathology, 2009

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An SRY-negative XX male with Huriez syndrome

alessandro terrinoni

Clinical Genetics, 2001

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Lower Urinary Tract Dysfunction in Children

Aart Klijn

European Urology Supplements, 2012

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Structural and functional analysis of mutations in alkaptonuria

Olga Criado

Human Molecular Genetics, 2000

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