Bilateral preaxial polydactyly in a WAGR syndrome patient-Reference-Cited by-同舟云学术

Bilateral preaxial polydactyly in a WAGR syndrome patient

Published:2005 Issue:4 Volume:134A Page:426-429
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Manoukian Siranoush,Crolla John A.,Mammoliti Palma M.A.,Testi Maria Adele,Zanini Rinaldo,Carpanelli Maria Luisa,Piozzi Elena,Sozzi Gabriella,De Vecchi Giovanna,Terenziani Monica,Spreafico Filippo,Collini Paola,Radice Paolo,Perotti Daniela

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference23 articles.

1. Polydactyly: How many disorders and how many genes?

2. Wilms Tumor Locus on 11p13 Defined by Multiple CpG Island-Associated Transcripts

3. Characteristics and Outcomes of Children With the Wilms Tumor-Aniridia Syndrome: A Report From the National Wilms Tumor Study Group

4. Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus

5. Frequent Chromosome Aberrations Revealed by Molecular Cytogenetic Studies in Patients with Aniridia

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Characterization of Associated Nonclassical Phenotypes in Patients with Deletion in the WAGR Region Identified by Chromosomal Microarray: New Insights and Literature Review;Molecular Syndromology;2022-02-11

2. Abnormal WT1 expression in human fetuses with bilateral renal agenesis and cardiac malformations;Birth Defects Research Part A: Clinical and Molecular Teratology;2012-01-13

3. WAGR Syndrome;Management of Genetic Syndromes;2010-05-17

4. A novel WT1 mutation in a 46,XY boy with congenital bilateral cryptorchidism, nystagmus and Wilms tumor;Pediatric Nephrology;2009-07