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Detection of Monosomy 7 and Trisomy 8 in Myeloid Neoplasia: A Comparison of Banding and Fluorescence In Situ Hybridization

Blood, 1993-08, Vol.82 (3), p.904-913

1993

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Individuals with abnormal phenotype and normal G-banding karyotype: improvement and limitations in the diagnosis by the use of 24-colour FISH

Human genetics, 2000-04, Vol.106 (4), p.392-398

2000

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Combined immunophenotyping and DNA in situ hybridization to study lineage involvement in patients with myelodysplastic syndromes

Blood, 1992-04, Vol.79 (7), p.1823-1828

1992

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Evolution of acquired severe aplastic anaemia to myelodysplasia and subsequent leukaemia in adults

British journal of haematology, 1988-09, Vol.70 (1), p.55-62

1988

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RT-PCR Diagnosis of Patients With Acute Nonlymphocytic Leukemia and inv(16)(pl3q22) and Identification of New Alternative Splicing in CBFB-MYH11 Transcripts

Blood, 1995-07, Vol.86 (1), p.277-282

1995

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Prenatal diagnosis of trisomy 13 on fetal cells obtained from maternal blood after minor enrichment

Prenatal diagnosis, 1998-10, Vol.18 (10), p.1082-1085

1998

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Assessment of prenatal karyotypes

Human reproduction (Oxford), 2000-01, Vol.15 (1), p.228-229

2000

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Premature menopause because of an inherited deletion in the long arm of the X-chromosome

Fertility and sterility, 1991-03, Vol.55 (3), p.631-633

1991

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PRENATAL AND POSTNATAL INVESTIGATION OF A CASE WITH MILLER-DIEKER SYNDROME DUE TO A FAMILIAL CRYPTIC TRANSLOCATION t(17;20) (p13.3;q13.3) DETECTED BY FLUORESCENCE IN SITU HYBRIDIZATION

Prenatal diagnosis, 1997-02, Vol.17 (2), p.173-179

1997

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Effect of subcutaneously administered human recombinant erythropoietin on erythropoiesis in patients with myelodysplasia

British journal of haematology, 1991-08, Vol.78 (4), p.488-493

1991

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Two Distinct Loci on the Short Arm of Chromosome 16 Are Involved in Myeloid Leukemia

Blood, 1991-04, Vol.77 (7), p.1555-1559

1991

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A near false-negative finding of mosaic trisomy 21-a cautionary tale

Prenatal diagnosis, 1998-07, Vol.18 (7), p.742-746

1998

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Yet another variation on the theme of chromosome 18 heteromorphisms?

Prenatal diagnosis, 1997-06, Vol.17 (6), p.585-586

1997

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Combined GTG-banding and nonradioactive in situ hybridization improves characterization of complex karyotypes

Cytogenetic and genome research, 1990, Vol.54 (1-2), p.20-23

1990

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Proliferation and Cytogenetic Analysis of Hairy Cell Leukemia Upon Stimulation Via the CD40 Antigen

Blood, 1994-11, Vol.84 (9), p.3134-3141

1994

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The current state of research with peripheral tissues in Huntington disease

Human genetics, 1984-01, Vol.66 (2-3), p.115-131

Beverstock, G C

1984

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Monosomy 8p: an easily overlooked syndrome

Journal of medical genetics, 1986-04, Vol.23 (2), p.153-154

1986

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The fragile X syndrome in a large family. I. Cytogenetic and clinical investigations

Journal of medical genetics, 1987-01, Vol.24 (1), p.23-31

1987

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Absence of significant autosomal lesions in Huntington's disease

Annals of human genetics, 1985-10, Vol.49 (4), p.283-290

1985

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The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986

Clinical genetics, 1988-06, Vol.33 (6), p.410-417

1988

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Fetal blood group determination in first-trimester pregnancy for the management of severe immunization

American journal of obstetrics and gynecology, 1987-01, Vol.156 (1), p.120-123

1987

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T‐cell prolymphocytic leukemia with an unusual phenotype CD4+ CD8

Cancer, 1987-08, Vol.60 (4), p.794-803

1987

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Effect of Mast Cell Growth Factor (c-kit ligand) on Clonogenic Leukemic Precursor Cells

Blood, 1992-08, Vol.80 (3), p.750-757

1992

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Detection of fetal erythroblasts in maternal blood by one-step gradient enrichment and immunocytochemical recognition

Early human development, 1996-12, Vol.47 Suppl, p.S95-S97

1996

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Duplication in the proximal portion of the long arm of chromosome 15, in a girl without phenotypic features of the Prader-Willi syndrome

Clinical genetics, 1984-07, Vol.26 (1), p.65-68

1984

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Detection of Monosomy 7 and Trisomy 8 in Myeloid Neoplasia: A Comparison of Banding and Fluorescence In Situ Hybridization

Individuals with abnormal phenotype and normal G-banding karyotype: improvement and limitations in the diagnosis by the use of 24-colour FISH

Combined immunophenotyping and DNA in situ hybridization to study lineage involvement in patients with myelodysplastic syndromes

Evolution of acquired severe aplastic anaemia to myelodysplasia and subsequent leukaemia in adults

RT-PCR Diagnosis of Patients With Acute Nonlymphocytic Leukemia and inv(16)(pl3q22) and Identification of New Alternative Splicing in CBFB-MYH11 Transcripts

Prenatal diagnosis of trisomy 13 on fetal cells obtained from maternal blood after minor enrichment

Assessment of prenatal karyotypes

Premature menopause because of an inherited deletion in the long arm of the X-chromosome

PRENATAL AND POSTNATAL INVESTIGATION OF A CASE WITH MILLER-DIEKER SYNDROME DUE TO A FAMILIAL CRYPTIC TRANSLOCATION t(17;20) (p13.3;q13.3) DETECTED BY FLUORESCENCE IN SITU HYBRIDIZATION

Effect of subcutaneously administered human recombinant erythropoietin on erythropoiesis in patients with myelodysplasia

Two Distinct Loci on the Short Arm of Chromosome 16 Are Involved in Myeloid Leukemia

A near false-negative finding of mosaic trisomy 21-a cautionary tale

Yet another variation on the theme of chromosome 18 heteromorphisms?

Combined GTG-banding and nonradioactive in situ hybridization improves characterization of complex karyotypes

Proliferation and Cytogenetic Analysis of Hairy Cell Leukemia Upon Stimulation Via the CD40 Antigen

The current state of research with peripheral tissues in Huntington disease

Monosomy 8p: an easily overlooked syndrome

The fragile X syndrome in a large family. I. Cytogenetic and clinical investigations

Absence of significant autosomal lesions in Huntington's disease

The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986

Fetal blood group determination in first-trimester pregnancy for the management of severe immunization

T‐cell prolymphocytic leukemia with an unusual phenotype CD4+ CD8

Effect of Mast Cell Growth Factor (c-kit ligand) on Clonogenic Leukemic Precursor Cells

Detection of fetal erythroblasts in maternal blood by one-step gradient enrichment and immunocytochemical recognition

Duplication in the proximal portion of the long arm of chromosome 15, in a girl without phenotypic features of the Prader-Willi syndrome

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