Precise mapping of t(12;14) leiomyoma breakpoint on chromosome 14 between D14S298 and D14S540.

[1]  R. White,et al.  Breakpoint analysis: precise localization of genetic markers by means of nonstatistical computation using relatively few genotypes. , 1995, American journal of human genetics.

[2]  R. White,et al.  A strategy for constructing high-resolution genetic maps of the human genome: a genetic map of chromosome 17p, ordered with meiotic breakpoint-mapping panels. , 1995, American journal of human genetics.

[3]  T. Houseal,et al.  Physical mapping of the uterine leiomyoma t(12;14)(q13‐15;q24.1) breakpoint on chromosome 14 between SPTB and D14S77 , 1994, Genes, chromosomes & cancer.

[4]  J. Bullerdiek,et al.  Identification, molecular cloning, and characterization of the chromosome 12 breakpoint cluster region of uterine leiomyomas , 1994, Genes, chromosomes & cancer.

[5]  Cécile Fizames,et al.  The 1993–94 Généthon human genetic linkage map , 1994, Nature Genetics.

[6]  Aravinda Chakravarti,et al.  Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map , 1994, Nature Genetics.

[7]  J. Weber,et al.  Integrated human genome–wide maps constructed using the CEPH reference panel , 1994, Nature Genetics.

[8]  P. D. de Jong,et al.  Physical mapping of chromosome 12q breakpoints in lipoma, pleomorphic salivary gland adenoma, uterine leiomyoma, and myxoid liposarcoma. , 1994, Genomics.

[9]  F. Mitelman,et al.  Recombinations of chromosomal bands 6p21 and 14q24 characterise pulmonary hamartomas. , 1993, British Journal of Cancer.

[10]  J. Biegel,et al.  Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma , 1993, Nature Genetics.

[11]  G. Thomas,et al.  Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours , 1992, Nature.

[12]  F. Mitelman,et al.  High resolution mapping of consistent leiomyoma breakpoints in chromosomes 12 and 14 to 12q15 and 14q24.1 , 1990, Genes, chromosomes & cancer.

[13]  S. Heim,et al.  Uterine leiomyoma cytogenetics , 1990, Genes, chromosomes & cancer.

[14]  C. Turc‐Carel,et al.  Consistent breakpoints in region 14q22-q24 in uterine leiomyoma. , 1988, Cancer genetics and cytogenetics.

[15]  A. Sandberg,et al.  14q+ in Ph-positive chronic myelogenous leukemia. , 1986, Cancer genetics and cytogenetics.

[16]  S. Silverberg,et al.  Pathology in Gynecology and Obstetrics , 1985 .

[17]  J. Stephenson,et al.  Philadelphia chromosomal breakpoints are clustered within a limited region, bcr, on chromosome 22 , 1984, Cell.

[18]  T. Matise,et al.  Erratum: Automated construction of genetic linkage maps using an expert system (MultiMap): A human genome linkage map (Nature Genetics (1994) 6 (384- 390)) , 1994 .

[19]  H. Donis-Keller,et al.  A comprehensive genetic linkage map of the human genome. NIH/CEPH Collaborative Mapping Group. , 1992, Science.