Evidence That Lymphangiomyomatosis Is Caused by TSC2 Mutations: Chromosome 16p13 Loss of Heterozygosity in Angiomyolipomas and Lymph Nodes from Women with Lymphangiomyomatosis
- 1 April 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 62 (4) , 810-815
- https://doi.org/10.1086/301804
Abstract
No abstract availableKeywords
This publication has 39 references indexed in Scilit:
- Constitutional RB1-Gene Mutations in Patients with Isolated Unilateral RetinoblastomaAmerican Journal of Human Genetics, 1997
- Lymphangioleiomyomatosis and tuberous sclerosis: where is the border?European Respiratory Journal, 1996
- Extrathoracic angiomyolipomas in lymphangioleiomyomatosisEuropean Respiratory Journal, 1996
- A PCR-Based Genetic Linkage Map of Human Chromosome 16Genomics, 1994
- Angiomyolipoma of the kidney. Immunoreactivity with HMB‐45. Light‐ and electron‐microscopic findingsHistopathology, 1994
- Two loci for Tuberous Sclerosis: one on 9q34 and one on 16p13Annals of Human Genetics, 1994
- Identification and characterization of the tuberous sclerosis gene on chromosome 16Cell, 1993
- A High-Resolution Linkage Map of Human 9q34.1Genomics, 1993
- Characterization of the smooth muscle cell infiltrate and associated connective matrix of lymphangiomyomatosis. Immunohistochemical and ultrastructural study of two casesThe Journal of Pathology, 1992
- Mutation and Cancer: Statistical Study of RetinoblastomaProceedings of the National Academy of Sciences, 1971