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Atlas of Genetics and Cytogenetics in Oncology and Haematology, year 2003

Nucleic acids research, 2003-01, Vol.31 (1), p.272

2003

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CD30‐positive large cell lymphomas (‘Ki‐1 lymphoma’) are associated with a chromosomal translocation involving 5q35

British journal of haematology, 1990-02, Vol.74 (2), p.161-168

1990

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Atlas of genetics and cytogenetics in oncology and haematology, an interactive database

Nucleic acids research, 2000-01, Vol.28 (1), p.349

2000

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Atlas of Genetics and Cytogenetics in Oncology and Haematology, updated

Nucleic acids research, 2001-01, Vol.29 (1), p.303

2001

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AML1 overexpression and or mutations should be checked in trisomy 21 patients with megakaryocytic leukemia

Leukemia, 2003-07, Vol.17 (7), p.1421-1421

2003

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An Atlas on genes and chromosomes in oncology and haematology

Cellular and molecular biology (Noisy-le-Grand, France), 2004-11, Vol.50 (7), p.805

2004

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An atlas of chromosomes in hematological malignancies. Example: 11q23 and MLL partners

Leukemia, 2001-06, Vol.15 (6), p.987-989

2001

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Monosomy 21q: two cases of del(21q) and review of the literature

Clinical genetics, 1995-09, Vol.48 (3), p.140-147

1995

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beta $ Amyloid Gene Duplication in Alzheimer's Disease and Karyotypically Normal down Syndrome

Science (American Association for the Advancement of Science), 1987-03, Vol.235 (4794), p.1390-1392

1987

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A database on cytogenetics in haematology and oncology

Nucleic acids research, 1999-01, Vol.27 (1), p.353

1999

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Eleven new cases of del(9p) and features from 80 cases

Journal of medical genetics, 1988-11, Vol.25 (11), p.741-749

1988

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Protocols to establish genotype-phenotype correlations in down syndrome

American journal of human genetics, 1991-07, Vol.49 (1), p.207-235

1991

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Trisomy 8q due to i(8q) or der(8) t(8;8) is a frequent lesion in T‐prolymphocytic leukaemia: four new cases and a review of the literature

British journal of haematology, 1994-04, Vol.86 (4), p.780-785

1994

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Cytogenetic heterogeneity in t(11;19) acute leukemia : clinical, hematological and cytogenetic analyses of 48 patients : updated published cases and 16 new observations

Leukemia, 1993-02, Vol.7 (2), p.152-160

1993

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Complex translocations, simple variant translocations and Ph-negative cases in chronic myelogenous leukaemia

Human genetics, 1990-10, Vol.85 (6), p.565-568

Huret, J L

1990

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Chromosome 21 and platelets: a gene dosage effect?

Clinical genetics, 1997-02, Vol.51 (2), p.140-141

1997

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Presence of HBV DNA in spermatozoa: A possible vertical transmission of HBV via the germ line

Journal of medical virology, 1985-05, Vol.16 (1), p.61-66

1985

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Malignant Histiocytosis: A Specific t(2;5)(p23;q35) Translocation? Review of the Literature

Blood, 1988-09, Vol.72 (3), p.1045-1047

1988

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Nuclear Chromatin Decondensation of Human Sperm: A Review

Archives of andrology, 1986, Vol.16 (2), p.97-109

Huret, J. L.

1986

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Down syndrome with partial duplication and del (21) syndrome: study protocol and call for collaboration. Study I: clinical assessment

Clinical genetics, 1996-01, Vol.49 (1), p.20-27

1996

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Dicentric (9;12) in acute lymphocytic leukemia and other hematological malignancies: report from a dic(9;12) study group

Leukemia, 1995-01, Vol.9 (1), p.102-106

1995

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Down syndrome with duplication of a region of chromosome 21 containing the CuZn superoxide dismutase gene without detectable karyotypic abnormality

Human genetics, 1987-03, Vol.75 (3), p.251-257

1987

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Aberrant breakpoints in chronic myelogenous leukaemia; oncogenes and fragile sites

Human genetics, 1986-12, Vol.74 (4), p.447-448

1986

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Ring chromosome 21 in a phenotypically normal but infertile man

Clinical genetics, 1985-12, Vol.28 (6), p.541-545

1985

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INV(12) (p13q11) and dicentric chromosomes in a secondary leukaemia with basophilia

Haematologica (Roma), 1990-09, Vol.75 (5), p.473

1990

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Atlas of Genetics and Cytogenetics in Oncology and Haematology, year 2003

CD30‐positive large cell lymphomas (‘Ki‐1 lymphoma’) are associated with a chromosomal translocation involving 5q35

Atlas of genetics and cytogenetics in oncology and haematology, an interactive database

Atlas of Genetics and Cytogenetics in Oncology and Haematology, updated

AML1 overexpression and or mutations should be checked in trisomy 21 patients with megakaryocytic leukemia

An Atlas on genes and chromosomes in oncology and haematology

An atlas of chromosomes in hematological malignancies. Example: 11q23 and MLL partners

Monosomy 21q: two cases of del(21q) and review of the literature

beta $ Amyloid Gene Duplication in Alzheimer's Disease and Karyotypically Normal down Syndrome

A database on cytogenetics in haematology and oncology

Eleven new cases of del(9p) and features from 80 cases

Protocols to establish genotype-phenotype correlations in down syndrome

Trisomy 8q due to i(8q) or der(8) t(8;8) is a frequent lesion in T‐prolymphocytic leukaemia: four new cases and a review of the literature

Cytogenetic heterogeneity in t(11;19) acute leukemia : clinical, hematological and cytogenetic analyses of 48 patients : updated published cases and 16 new observations

Complex translocations, simple variant translocations and Ph-negative cases in chronic myelogenous leukaemia

Chromosome 21 and platelets: a gene dosage effect?

Presence of HBV DNA in spermatozoa: A possible vertical transmission of HBV via the germ line

Malignant Histiocytosis: A Specific t(2;5)(p23;q35) Translocation? Review of the Literature

Nuclear Chromatin Decondensation of Human Sperm: A Review

Down syndrome with partial duplication and del (21) syndrome: study protocol and call for collaboration. Study I: clinical assessment

Dicentric (9;12) in acute lymphocytic leukemia and other hematological malignancies: report from a dic(9;12) study group

Down syndrome with duplication of a region of chromosome 21 containing the CuZn superoxide dismutase gene without detectable karyotypic abnormality

Aberrant breakpoints in chronic myelogenous leukaemia; oncogenes and fragile sites

Ring chromosome 21 in a phenotypically normal but infertile man

INV(12) (p13q11) and dicentric chromosomes in a secondary leukaemia with basophilia

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