Expanding the spectrum of the Perlman syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference9 articles.
1. Bilateral nephroblastomatosis
2. The Perlman familial nephroblastomatosis syndrome
3. Metanephric hamartomas and nephroblastomatosis in siblings
4. The Fryns syndrome: diaphragmatic defects, craniofacial dysmorphism, and distal digital hypoplasia Further evidence for autosomal recessive inheritance
5. The Perlman syndrome: Familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies
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2. Molecular Mechanisms Contributing to the Etiology of Congenital Diaphragmatic Hernia: A Review and Novel Cases;The Journal of Pediatrics;2022-07
3. A Rare Coexistence of Bilateral Congenital Wilms Tumor with Ductal Plate Malformation at Autopsy;Fetal and Pediatric Pathology;2016-04-07
4. Genetic Counseling for Childhood Tumors and Inherited Cancer-Predisposing Syndromes;The Surgery of Childhood Tumors;2016
5. The genetics of common disorders – Congenital diaphragmatic hernia;European Journal of Medical Genetics;2014-08
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