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Genetic profiles of gastroesophageal cancer: combined analysis using expression array and tiling array–comparative genomic hybridization

Cancer genetics and cytogenetics, 2010-07, Vol.200 (2), p.120-126

2010

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6q deletion discriminates Waldenström macroglobulinemia from IgM monoclonal gammopathy of undetermined significance

Cancer genetics and cytogenetics, 2006-09, Vol.169 (2), p.150-153

2006

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PEG10 is a probable target for the amplification at 7q21 detected in hepatocellular carcinoma

Cancer genetics and cytogenetics, 2010-04, Vol.198 (2), p.118-125

2010

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Chromosome 6 abnormalities are recurrent in synovial chondromatosis

Cancer genetics and cytogenetics, 2003, Vol.140 (1), p.18-22

2003

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Detection of human papillomavirus genotypes with liquid bead microarray in cervical lesions of northern Chinese patients

Cancer genetics and cytogenetics, 2008-04, Vol.182 (1), p.12-17

2008

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6p21 rearrangements in uterine leiomyomas targeting HMGA1

Cancer genetics and cytogenetics, 2010-12, Vol.203 (2), p.247-252

2010

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The t(6;9)(p22;q34) in myeloid neoplasms: a retrospective study of 16 cases

Cancer genetics and cytogenetics, 2010-12, Vol.203 (2), p.297-302

2010

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A subgroup of malignant fibrous histiocytomas is associated with genetic changes similar to those of well-differentiated liposarcomas

Cancer genetics and cytogenetics, 2002-11, Vol.139 (1), p.24-29

2002

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Correlation between 6q25.3 deletion status and survival in pediatric intracranial ependymomas

Cancer genetics and cytogenetics, 2008-04, Vol.182 (1), p.18-26

2008

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ETV6–ARNT fusion in a patient with childhood T lymphoblastic leukemia

Cancer genetics and cytogenetics, 2010-10, Vol.202 (1), p.22-26

2010

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Molecular analysis of germline t(3;6) and t(3;12) associated with conventional renal cell carcinomas indicates their rate-limiting role and supports the three-hit model of carcinogenesis

Cancer genetics and cytogenetics, 2010-08, Vol.201 (1), p.15-23

2010

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Translocation (6;13)(p21;q14.1) as a rare nonrandom cytogenetic abnormality in chronic lymphocytic leukemia

Cancer genetics and cytogenetics, 2010-04, Vol.198 (1), p.66-70

2010

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B lymphoblastic leukemia with ETV6 amplification

Cancer genetics and cytogenetics, 2010-12, Vol.203 (2), p.284-287

2010

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Genomic alterations in primary cutaneous melanomas detected by metaphase comparative genomic hybridization with laser capture or manual microdissection: 6p gains may predict poor outcome

Cancer genetics and cytogenetics, 2005-02, Vol.157 (1), p.1-11

2005

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Molecular cytogenetic analysis of Korean patients with Waldenström macroglobulinemia

Cancer genetics and cytogenetics, 2010-03, Vol.197 (2), p.117-121

2010

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Chromosome band 6q deletion pattern in malignant lymphomas

Cancer genetics and cytogenetics, 2006-03, Vol.165 (2), p.106-113

2006

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Cytogenetic and array comparative genomic hybridization analysis of a series of hepatoblastomas

Cancer genetics and cytogenetics, 2009-10, Vol.194 (2), p.82-87

2009

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Cytogenetic and molecular genetic analyses of endometrial stromal sarcoma: nonrandom involvement of chromosome arms 6p and 7p and confirmation of JAZF1/ JJAZ1 gene fusion in t(7;17)

Cancer genetics and cytogenetics, 2003-07, Vol.144 (2), p.119-124

2003

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Chromosomal rearrangements in lipofibromatosis

Cancer genetics and cytogenetics, 2007-12, Vol.179 (2), p.136-139

2007

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MNX1–ETV6 fusion gene in an acute megakaryoblastic leukemia and expression of the MNX1 gene in leukemia and normal B cell lines

Cancer genetics and cytogenetics, 2008-10, Vol.186 (2), p.115-119

2008

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A complex translocation (6;12;8)(q25;q24.3;q13) in a fibrous hamartoma of infancy

Cancer genetics and cytogenetics, 2006-12, Vol.171 (2), p.115-118

2006

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Prognostic significance of trisomy 6 in an adult acute myeloid leukemia with t(8;21)

Cancer genetics and cytogenetics, 2010-10, Vol.202 (2), p.141-143

2010

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CASP8AP2 is a novel partner gene of MLL rearrangement with t(6;11)(q15;q23) in acute myeloid leukemia

Cancer genetics and cytogenetics, 2009-11, Vol.195 (1), p.94-95

2009

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Novel 6p rearrangements and recurrent translocation breakpoints in retinoblastoma cell lines identified by spectral karyotyping and mBAND analyses

Cancer genetics and cytogenetics, 2007-12, Vol.179 (2), p.102-111

2007

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Chondromyxoid fibroma of the nasal cavity with an interstitial insertion between chromosomes 6 and 19

Cancer genetics and cytogenetics, 2006-12, Vol.171 (2), p.97-100

2006

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Genetic profiles of gastroesophageal cancer: combined analysis using expression array and tiling array–comparative genomic hybridization

6q deletion discriminates Waldenström macroglobulinemia from IgM monoclonal gammopathy of undetermined significance

PEG10 is a probable target for the amplification at 7q21 detected in hepatocellular carcinoma

Chromosome 6 abnormalities are recurrent in synovial chondromatosis

Detection of human papillomavirus genotypes with liquid bead microarray in cervical lesions of northern Chinese patients

6p21 rearrangements in uterine leiomyomas targeting HMGA1

The t(6;9)(p22;q34) in myeloid neoplasms: a retrospective study of 16 cases

A subgroup of malignant fibrous histiocytomas is associated with genetic changes similar to those of well-differentiated liposarcomas

Correlation between 6q25.3 deletion status and survival in pediatric intracranial ependymomas

ETV6–ARNT fusion in a patient with childhood T lymphoblastic leukemia

Molecular analysis of germline t(3;6) and t(3;12) associated with conventional renal cell carcinomas indicates their rate-limiting role and supports the three-hit model of carcinogenesis

Translocation (6;13)(p21;q14.1) as a rare nonrandom cytogenetic abnormality in chronic lymphocytic leukemia

B lymphoblastic leukemia with ETV6 amplification

Genomic alterations in primary cutaneous melanomas detected by metaphase comparative genomic hybridization with laser capture or manual microdissection: 6p gains may predict poor outcome

Molecular cytogenetic analysis of Korean patients with Waldenström macroglobulinemia

Chromosome band 6q deletion pattern in malignant lymphomas

Cytogenetic and array comparative genomic hybridization analysis of a series of hepatoblastomas

Cytogenetic and molecular genetic analyses of endometrial stromal sarcoma: nonrandom involvement of chromosome arms 6p and 7p and confirmation of JAZF1/ JJAZ1 gene fusion in t(7;17)

Chromosomal rearrangements in lipofibromatosis

MNX1–ETV6 fusion gene in an acute megakaryoblastic leukemia and expression of the MNX1 gene in leukemia and normal B cell lines

A complex translocation (6;12;8)(q25;q24.3;q13) in a fibrous hamartoma of infancy

Prognostic significance of trisomy 6 in an adult acute myeloid leukemia with t(8;21)

CASP8AP2 is a novel partner gene of MLL rearrangement with t(6;11)(q15;q23) in acute myeloid leukemia

Novel 6p rearrangements and recurrent translocation breakpoints in retinoblastoma cell lines identified by spectral karyotyping and mBAND analyses

Chondromyxoid fibroma of the nasal cavity with an interstitial insertion between chromosomes 6 and 19

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