1q42∼q44 is rarely cytogenetically involved in sporadic uterine leiomyomata
- 1 October 2002
- journal article
- other
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 138 (1) , 92-93
- https://doi.org/10.1016/s0165-4608(02)00585-x
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Familial Cutaneous Leiomyomatosis Is a Two-Hit Condition Associated with Renal Cell Cancer of Characteristic HistopathologyThe American Journal of Pathology, 2001
- Localization of a Gene (MCUL1) for Multiple Cutaneous Leiomyomata and Uterine Fibroids to Chromosome 1q42.3-q43American Journal of Human Genetics, 2001
- Inherited susceptibility to uterine leiomyomas and renal cell cancerProceedings of the National Academy of Sciences, 2001
- Genetics of uterine leiomyomataGenes, Chromosomes and Cancer, 2000
- Allelotype of Uterine LeiomyomasCancer Genetics and Cytogenetics, 1999
- Deletion of HMG17 in Uterine Leiomyomas with Ring Chromosome 1Cancer Genetics and Cytogenetics, 1999
- Translocations in 7q22 define a critical region in uterine leiomyomataCancer Genetics and Cytogenetics, 1994
- Is the chromosome band 1p36 another hot‐spot for rearrangements in uterine leiomyoma?Genes, Chromosomes and Cancer, 1990