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A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia

Leukemia, 2001-10, Vol.15 (10), p.1495-1504

2001

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High Frequency of t(12;21) in Childhood B-Lineage Acute Lymphoblastic Leukemia

Blood, 1995-12, Vol.86 (11), p.4263-4269

1995

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The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion

Blood, 1995-06, Vol.85 (12), p.3662-3670

1995

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AF6q21, a Novel Partner of the MLL Gene in t(6; 11)(q21; q23), Defines a Forkhead Transcriptional Factor Subfamily

Blood, 1997-11, Vol.90 (9), p.3714-3719

1997

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t( 12;21): A new recurrent translocation in acute lymphoblastic leukemia

Genes chromosomes & cancer, 1994-03, Vol.9 (3), p.186-191

1994

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The TEL gene products: nuclear phosphoproteins with DNA binding properties

Oncogene, 1997-01, Vol.14 (3), p.349-357

1997

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Assignment of the TCF-4 gene (TCF7L2) to human chromosome band 10q25.3

Cytogenetics and cell genetics, 2000, Vol.88 (3-4), p.264

2000

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Deletion of the short arm of chromosome 12 is a secondary event in acute lymphoblastic leukemia with t(12;21)

Leukemia, 1996, Vol.10 (1), p.167-170

1996

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Faconi anemia and bone marrow clonal chromosome abnormalities

Leukemia, 1996-11, Vol.10 (11), p.1700-1704

1996

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A minority of 46,XX true hermaphrodites are positive for the Y-DNA sequence including SRY

Human genetics, 1992-09, Vol.90 (1-2), p.121-125

1992

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Cytogenetic Studies in Acute Promyelocytic Leukemia: A Survey of Secondary Chromosomal Abnormalities

Genes chromosomes & cancer, 1991-09, Vol.3 (5), p.332-337

1991

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Partial chromosome 21 amplification in a child with acute lymphoblastic leukemia

Genes chromosomes & cancer, 1995-11, Vol.14 (3), p.204-209

1995

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Ph1+bcr- acute leukemias: implication of Alu sequences in a chromosomal translocation occurring in the new cluster region within the BCR gene

Oncogene, 1989-02, Vol.4 (2), p.195-202

1989

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Chromosomal localization of the human D3 dopamine receptor gene

Human genetics, 1991-09, Vol.87 (5), p.618-620

1991

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Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome

Comptes rendus de l'Académie des sciences, Série III, Sciences de la vie, 1993, Vol.316 (4), p.375

1993

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A new breakpoint, telomeric to TEL/ETV6, on the short arm of chromosome 12 in T cell acute lymphoblastic leukemia

Leukemia, 1997-08, Vol.11 (8), p.1360-1363

1997

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An interstitial 11q23 deletion proven to be a rearrangement interrupting the MLL gene in an infant with acute myeloblastic leukemia

Leukemia, 1996-11, Vol.10 (11), p.1844-1846

1996

Volltextzugriff (PDF)

Genomic Organization of the Human ERM (ETV5) Gene, a PEA3 Group Member of ETS Transcription Factors

Genomics (San Diego, Calif.), 1996-07, Vol.35 (1), p.236-240

1996

Volltextzugriff (PDF)

In situ hybridization to interphase nuclei in acute leukemia

Genes chromosomes & cancer, 1993-10, Vol.8 (2), p.98-103

1993

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The 5-HT2B Receptor Gene Maps to 2q36.3–2q37.1

Genomics (San Diego, Calif.), 1996-02, Vol.32 (1), p.172-173

1996

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Human and mouse Krüppel-like (MOK2) orthologue genes encode two different zinc finger proteins

Journal of molecular evolution, 1995-12, Vol.41 (6), p.784-794

1995

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Secondary acute myeloblastic leukemia with t(16;21)(q24;q22) involving the AML1 gene

Hematology and cell therapy, 1996-04, Vol.38 (2), p.183-186

1996

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FISH analysis of translocations involving the short arm of chromosome 9 in lymphoid malignancies

Genes chromosomes & cancer, 1997-08, Vol.19 (4), p.273-277

1997

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Inversion-associated translocations in acute myelomonocytic leukemia with eosinophilia

Genes chromosomes & cancer, 1995-01, Vol.12 (1), p.58-62

1995

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Chromosome microdissection in leukemia: A powerful tool for the analysis of complex chromosomal rearrangements

Genes chromosomes & cancer, 1996-01, Vol.15 (1), p.26-33

1996

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A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia

High Frequency of t(12;21) in Childhood B-Lineage Acute Lymphoblastic Leukemia

The t(12;21) of acute lymphoblastic leukemia results in a tel-AML1 gene fusion

AF6q21, a Novel Partner of the MLL Gene in t(6; 11)(q21; q23), Defines a Forkhead Transcriptional Factor Subfamily

t( 12;21): A new recurrent translocation in acute lymphoblastic leukemia

The TEL gene products: nuclear phosphoproteins with DNA binding properties

Assignment of the TCF-4 gene (TCF7L2) to human chromosome band 10q25.3

Deletion of the short arm of chromosome 12 is a secondary event in acute lymphoblastic leukemia with t(12;21)

Faconi anemia and bone marrow clonal chromosome abnormalities

A minority of 46,XX true hermaphrodites are positive for the Y-DNA sequence including SRY

Cytogenetic Studies in Acute Promyelocytic Leukemia: A Survey of Secondary Chromosomal Abnormalities

Partial chromosome 21 amplification in a child with acute lymphoblastic leukemia

Ph1+bcr- acute leukemias: implication of Alu sequences in a chromosomal translocation occurring in the new cluster region within the BCR gene

Chromosomal localization of the human D3 dopamine receptor gene

Familial case of 46,XX male and 46,XX true hermaphrodite associated with a paternal-derived SRY-bearing X chromosome

A new breakpoint, telomeric to TEL/ETV6, on the short arm of chromosome 12 in T cell acute lymphoblastic leukemia

An interstitial 11q23 deletion proven to be a rearrangement interrupting the MLL gene in an infant with acute myeloblastic leukemia

Genomic Organization of the Human ERM (ETV5) Gene, a PEA3 Group Member of ETS Transcription Factors

In situ hybridization to interphase nuclei in acute leukemia

The 5-HT2B Receptor Gene Maps to 2q36.3–2q37.1

Human and mouse Krüppel-like (MOK2) orthologue genes encode two different zinc finger proteins

Secondary acute myeloblastic leukemia with t(16;21)(q24;q22) involving the AML1 gene

FISH analysis of translocations involving the short arm of chromosome 9 in lymphoid malignancies

Inversion-associated translocations in acute myelomonocytic leukemia with eosinophilia

Chromosome microdissection in leukemia: A powerful tool for the analysis of complex chromosomal rearrangements

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