Diaphragmatic hernia in Denys-Drash syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference21 articles.
1. Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome
2. Optimal conditions for directly sequencing double-stranded PCR products with Sequenase
3. The role of WT1 in Wilms tumorigenesis
4. Denys-Drash syndrome: Relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1
5. Patterns of malformation in children with congenital diaphragmatic defects
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1. Role of genetics and the environment in the etiology of congenital diaphragmatic hernia;World Journal of Pediatric Surgery;2024-08
2. Congenital diaphragmatic eventration with pulmonary dysplasia in Frasier syndrome due to a WT1 mutation of c.1432+5(IVS9)G>A;European Journal of Medical Genetics;2022-12
3. Identifying phenotypic expansions for congenital diaphragmatic hernia plus ( CDH +) using DECIPHER data;American Journal of Medical Genetics Part A;2022-07-29
4. Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing Challenge;Frontiers in Pediatrics;2022-02-03
5. Underlying genetic etiologies of congenital diaphragmatic hernia;Prenatal Diagnosis;2022-01-22
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