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Analysis of a new homozygous deletion in the tumor suppressor region at 3p12.3 reveals two novel intronic noncoding RNA genes

Genes chromosomes & cancer, 2006-07, Vol.45 (7), p.676-691

2006

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Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancer

Nature (London), 1987-12, Vol.330 (6148), p.578-581

1987

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FISH and array‐CGH analysis of a complex chromosome 3 aberration suggests that loss of CNTN4 and CRBN contributes to mental retardation in 3pter deletions

American journal of medical genetics. Part A, 2006-11, Vol.140A (22), p.2482-2487

2006

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Localization and intron usage analysis of the human CPT1B gene for muscle type carnitine palmitoyltransferase I

Biochimica et biophysica acta, 1997-05, Vol.1352 (2), p.123-128

1997

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Functional analysis of lung tumor suppressor activity at 3p21.3

Genes chromosomes & cancer, 2006-12, Vol.45 (12), p.1077-1093

2006

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An Evolutionary Rearrangement of the Xp11.3–11.23 Region in 3p21.3, a Region Frequently Deleted in a Variety of Cancers

Genomics (San Diego, Calif.), 1999-09, Vol.60 (2), p.238-240

1999

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A gene from human chromosome region 3p21 with reduced expression in small cell lung cancer

Cancer research (Chicago, Ill.), 1992-03, Vol.52 (6), p.1536-1541

1992

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Characterization of three new variant type cell lines derived from small cell carcinoma of the lung

Cancer research (Chicago, Ill.), 1985-12, Vol.45 (12), p.6024-6033

1985

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A homozygous deletion in a small cell lung cancer cell line involving a 3p21 region with a marked instability in yeast artificial chromosomes

Cancer research (Chicago, Ill.), 1994-08, Vol.54 (15), p.4183-4187

1994

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Deletion of the multidrug resistance protein MRP1 gene in acute myeloid leukemia: the impact on MRP activity

Blood, 2000-06, Vol.95 (11), p.3514-3519

2000

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Deletion of the multidrug resistance protein MRP1 gene in acute myeloid leukemia: the impact on MRP activity

Blood, 2000-06, Vol.95 (11), p.3514-3519

2000

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Cytogenetics of a malignant ovarian germ‐cell tumor

International journal of cancer, 1998-07, Vol.77 (2), p.217-218

1998

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Normal FHIT transcripts in renal cell cancer- and lung cancer-derived cell lines, including a cell line with a homozygous deletion in the FRA3B region

Genes chromosomes & cancer, 1997-08, Vol.19 (4), p.220-227

1997

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Allelic gains and losses in distinct regions of chromosome 6 in gastric carcinoma

Cancer genetics and cytogenetics, 2001-11, Vol.131 (1), p.54-59

2001

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Loss of the Y-Chromosome in the Primary Metastasis of a Male Sex Cord Stromal Tumor: Pathogenetic Implications

Cancer genetics and cytogenetics, 1999-07, Vol.112 (1), p.21-25

1999

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Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22

American journal of medical genetics, 1999-09, Vol.86 (2), p.168-173

1999

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NormalFHIT transcripts in renal cell cancer- and lung cancer-derived cell lines, including a cell line with a homozygous deletion in the FRA3B region

Genes chromosomes & cancer, 1997-08, Vol.19 (4), p.220-227

1997

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Defining the position of the breakpoint of the constitutional t(3;6) occurring in a family with renal cell carcinoma

Genes chromosomes & cancer, 1995-03, Vol.12 (3), p.224-228

1995

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Assignment of the gene coding for human cytochrome c oxidase subunit VIb to chromosome 19, band q13.1, by fluorescence in situ hybridization

Human genetics, 1991-07, Vol.87 (3), p.325-327

1991

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Ordering of markers in the pericentromeric region of chromosome 10

Human genetics, 1995-07, Vol.96 (1), p.116-118

1995

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Physical localisation of the chromosomal marker D13S31 places the Wilson disease locus at the junction of bands q14.3 and q21.1 of chromosome 13

Human genetics, 1993-06, Vol.91 (5), p.504-506

1993

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Identification of a tumor marker chromosome by flow sorting, DNA amplification in vitro, and in situ hybridization of the amplified product

Genes chromosomes & cancer, 1993-01, Vol.6 (1), p.10-16

1993

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Localization of DNA probes with tight linkage to the cystic fibrosis locus by in situ hybridization using fibroblasts with a 7q22 deletion

Human genetics, 1988-10, Vol.80 (2), p.161-164

1988

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Infantile and adult testicular germ cell tumors: a different pathogenesis?

Cancer genetics and cytogenetics, 2002-05, Vol.135 (1), p.57-62

2002

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Localization at a subband level of polymorphic 13q14 DNA probes for diagnosis of hereditary retinoblastoma and Wilson disease

Human genetics, 1987-12, Vol.77 (4), p.335-337

1987

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Analysis of a new homozygous deletion in the tumor suppressor region at 3p12.3 reveals two novel intronic noncoding RNA genes

Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancer

FISH and array‐CGH analysis of a complex chromosome 3 aberration suggests that loss of CNTN4 and CRBN contributes to mental retardation in 3pter deletions

Localization and intron usage analysis of the human CPT1B gene for muscle type carnitine palmitoyltransferase I

Functional analysis of lung tumor suppressor activity at 3p21.3

An Evolutionary Rearrangement of the Xp11.3–11.23 Region in 3p21.3, a Region Frequently Deleted in a Variety of Cancers

A gene from human chromosome region 3p21 with reduced expression in small cell lung cancer

Characterization of three new variant type cell lines derived from small cell carcinoma of the lung

A homozygous deletion in a small cell lung cancer cell line involving a 3p21 region with a marked instability in yeast artificial chromosomes

Deletion of the multidrug resistance protein MRP1 gene in acute myeloid leukemia: the impact on MRP activity

Deletion of the multidrug resistance protein MRP1 gene in acute myeloid leukemia: the impact on MRP activity

Cytogenetics of a malignant ovarian germ‐cell tumor

Normal FHIT transcripts in renal cell cancer- and lung cancer-derived cell lines, including a cell line with a homozygous deletion in the FRA3B region

Allelic gains and losses in distinct regions of chromosome 6 in gastric carcinoma

Loss of the Y-Chromosome in the Primary Metastasis of a Male Sex Cord Stromal Tumor: Pathogenetic Implications

Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22

NormalFHIT transcripts in renal cell cancer- and lung cancer-derived cell lines, including a cell line with a homozygous deletion in the FRA3B region

Defining the position of the breakpoint of the constitutional t(3;6) occurring in a family with renal cell carcinoma

Assignment of the gene coding for human cytochrome c oxidase subunit VIb to chromosome 19, band q13.1, by fluorescence in situ hybridization

Ordering of markers in the pericentromeric region of chromosome 10

Physical localisation of the chromosomal marker D13S31 places the Wilson disease locus at the junction of bands q14.3 and q21.1 of chromosome 13

Identification of a tumor marker chromosome by flow sorting, DNA amplification in vitro, and in situ hybridization of the amplified product

Localization of DNA probes with tight linkage to the cystic fibrosis locus by in situ hybridization using fibroblasts with a 7q22 deletion

Infantile and adult testicular germ cell tumors: a different pathogenesis?

Localization at a subband level of polymorphic 13q14 DNA probes for diagnosis of hereditary retinoblastoma and Wilson disease

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