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High-resolution genomic profiling of adenomas and carcinomas of the salivary glands reveals amplification, rearrangement, and fusion of HMGA2

Genes chromosomes & cancer, 2009-01, Vol.48 (1), p.69-82

2009

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High-resolution array CGH analysis of salivary gland tumors reveals fusion and amplification of the FGFR1 and PLAG1 genes in ring chromosomes

Oncogene, 2008-05, Vol.27 (21), p.3072-3080

2008

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Fusion of the NH2-Terminal domain of the basic helix-loop-helix protein TCF12 to TEC in extraskeletal myxoid chondrosarcoma with translocation t(9;15)(q22;q21)

Cancer research (Chicago, Ill.), 2000-12, Vol.60 (24), p.6832-6835

2000

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Conserved mechanism of PLAG1 activation in salivary gland tumors with and without chromosome 8q12 abnormalities : Identification of SII as a new fusion partner gene

Cancer research (Chicago, Ill.), 1999-02, Vol.59 (4), p.918-923

1999

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Karyotypic evolution in a human mucoepidermoid carcinoma

Hereditas, 1989-01, Vol.110 (1), p.75-78

1989

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Fusion of the NH2-terminal domain of the bHLH protein TCF12 to TEC in extraskeletal myxoid chondrosarcoma with translocation t(9; 15)(q22; q21)

Nature genetics, 2001-04, Vol.27 (S4), p.87-87

2001

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Translocation(11;19)(q14–21;p12) in a parotid mucoepidermoid carcinoma of a child

Cancer genetics and cytogenetics, 1995-02, Vol.79 (2), p.188-188

1995

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Cytogenetical observations in a cultured polymorphous low-grade adenocarcinoma originating from the minor salivary glands

Anticancer research, 1997-01, Vol.17 (1A), p.105

1997

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Karyotypic variability and evolutionary characteristics of a polymorphous low grade adenocarcinoma in the parotid gland

Cancer genetics and cytogenetics, 1991-08, Vol.55 (1), p.19-29

1991

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Chromosome studies in thyroid neoplasia

Cancer, 1989-08, Vol.64 (3), p.680-685

1989

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Characterisation of a cell line (LCC-18) from a cultured human neuroendocrine-differentiated colonic carcinoma

European journal of cancer & clinical oncology, 1991, Vol.27 (12), p.1663-1668

1991

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Similar chromosomal evolution in a uterine stromomyosarcoma and in one of two leiomyomas from the same patient

APMIS : acta pathologica, microbiologica et immunologica Scandinavica, 1989-01, Vol.97 (1-6), p.143-146

1989

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Impact of the in vitro technique used on the cytogenetic patterns in pleomorphic adenomas

Cancer genetics and cytogenetics, 1997-05, Vol.95 (1), p.9-15

1997

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Chromosomal patterns in human benign uterine leiomyomas

Cancer genetics and cytogenetics, 1990, Vol.44 (1), p.1-13

1990

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Significance of the choice of tissue culture technique on the chromosomal patterns in human mixed salivary gland tumors

Cancer genetics and cytogenetics, 1988-07, Vol.33 (2), p.229-244

1988

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Cytogenetic relationship between uterine lipoleiomyomas and typical leiomyomas

Virchows Archiv. Abteilung B. Zellpathologie, 1989, Vol.57 (1), p.77-79

1989

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Cytogenetic observations in a human gastric leiomyosarcoma

Cancer genetics and cytogenetics, 1989-02, Vol.37 (2), p.215-220

1989

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Human benign chondroblastoma with a pseudodiploid stemline characterized by a complex and balanced translocation

Cancer genetics and cytogenetics, 1992, Vol.58 (1), p.14-17

1992

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Mutational spectrum of the steroid 21-hydroxylase gene in Sweden : implications for genetic diagnosis and association with disease manifestation

The journal of clinical endocrinology and metabolism, 1994-05, Vol.78 (5), p.1145-1152

1994

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Steroid 21-Hydroxylase Deficiency: Three Additional Mutated Alleles and Establishment of Phenotype-Genotype Relationships of Common Mutations

Proceedings of the National Academy of Sciences - PNAS, 1992-08, Vol.89 (15), p.7232-7236

1992

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Characterization of mutations on the rare duplicated C4/CYP21 haplotype in steroid 21-hydroxylase deficiency

Human genetics, 1994-07, Vol.94 (1), p.50-54

1994

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Mutational Spectrum of the Steroid 21-Hydroxylase Gene In Sweden: Implications for Genetic Diagnosis and Association With Disease Manifestation

Obstetrical & gynecological survey, 1994-10, Vol.49 (10), p.695-697

1994

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High-resolution genomic profiling of adenomas and carcinomas of the salivary glands reveals amplification, rearrangement, and fusion of HMGA2

High-resolution array CGH analysis of salivary gland tumors reveals fusion and amplification of the FGFR1 and PLAG1 genes in ring chromosomes

Fusion of the NH2-Terminal domain of the basic helix-loop-helix protein TCF12 to TEC in extraskeletal myxoid chondrosarcoma with translocation t(9;15)(q22;q21)

Conserved mechanism of PLAG1 activation in salivary gland tumors with and without chromosome 8q12 abnormalities : Identification of SII as a new fusion partner gene

Karyotypic evolution in a human mucoepidermoid carcinoma

Fusion of the NH2-terminal domain of the bHLH protein TCF12 to TEC in extraskeletal myxoid chondrosarcoma with translocation t(9; 15)(q22; q21)

Translocation(11;19)(q14–21;p12) in a parotid mucoepidermoid carcinoma of a child

Cytogenetical observations in a cultured polymorphous low-grade adenocarcinoma originating from the minor salivary glands

Karyotypic variability and evolutionary characteristics of a polymorphous low grade adenocarcinoma in the parotid gland

Chromosome studies in thyroid neoplasia

Characterisation of a cell line (LCC-18) from a cultured human neuroendocrine-differentiated colonic carcinoma

Similar chromosomal evolution in a uterine stromomyosarcoma and in one of two leiomyomas from the same patient

Impact of the in vitro technique used on the cytogenetic patterns in pleomorphic adenomas

Chromosomal patterns in human benign uterine leiomyomas

Significance of the choice of tissue culture technique on the chromosomal patterns in human mixed salivary gland tumors

Cytogenetic relationship between uterine lipoleiomyomas and typical leiomyomas

Cytogenetic observations in a human gastric leiomyosarcoma

Human benign chondroblastoma with a pseudodiploid stemline characterized by a complex and balanced translocation

Mutational spectrum of the steroid 21-hydroxylase gene in Sweden : implications for genetic diagnosis and association with disease manifestation

Steroid 21-Hydroxylase Deficiency: Three Additional Mutated Alleles and Establishment of Phenotype-Genotype Relationships of Common Mutations

Characterization of mutations on the rare duplicated C4/CYP21 haplotype in steroid 21-hydroxylase deficiency

Mutational Spectrum of the Steroid 21-Hydroxylase Gene In Sweden: Implications for Genetic Diagnosis and Association With Disease Manifestation

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