A case of congenital aniridia and familial pheochromocytoma—With special reference to aniridia-Wilms' tumor syndrome
- 1 December 1982
- journal article
- research article
- Published by Springer Nature in Journal of Human Genetics
- Vol. 27 (4), 335-340
- https://doi.org/10.1007/bf01900445
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
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- One hundred cases of pheochromocytoma (107 tumors) at the columbia-presbyterian medical center, 1926-1976.A clinicopathological analysisCancer, 1977
- Aniridia-Wilms’ Tumour SyndromeOphthalmologica, 1977
- Computer-Assisted Analysis of Chromosomal Abnormalities: Detection of a Deletion in Aniridia/ Wilms' Tumor SyndromeScience, 1974
- Simultaneous occurrence of congenital aniridia, hamartoma, and Wilms' tumorThe Journal of Pediatrics, 1971
- Association of Wilms's Tumor with Aniridia, Hemihypertrophy and Other Congenital MalformationsNew England Journal of Medicine, 1964