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Carotid Stump Syndrome: Outcome from Surgical Management

European journal of vascular and endovascular surgery, 2001-03, Vol.21 (3), p.214-219

2001

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Mosaicism with a normal cell line and an autosomal structural rearrangement

Journal of medical genetics, 1994-02, Vol.31 (2), p.108-114

1994

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DNA sequence analysis of the major breakpoint cluster region of the BCR gene rearranged in Philadelphia-positive human leukemias

Oncogene, 1993-06, Vol.8 (6), p.1679-1683

1993

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Genomic diversity correlates with clinical variation in Ph′-negative chronic myeloid leukaemia

Nature (London), 1986-03, Vol.320 (6059), p.281-283

1986

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Essential thrombocythaemia and the Philadelphia chromosome

British journal of haematology, 1988-09, Vol.70 (1), p.13-19

1988

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Localization of the TRK proto-oncogene to human chromosome bands 1q23-1q24

Oncogene, 1991-06, Vol.6 (6), p.1093-1095

1991

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Telomeric association of chromosomes in B-cell lymphoid leukemia

Human genetics, 1984-01, Vol.67 (4), p.385-390

1984

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Effect of daylight on the reaction of thiols with Ellman's reagent, 5,5'-dithiobis(2-nitrobenzoic acid)

Clinical chemistry (Baltimore, Md.), 1987-10, Vol.33 (10), p.1928-1931

1987

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A Monoclonal Antibody Reacting With Human Basophils

Blood, 1987-05, Vol.69 (5), p.1414-1418

1987

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Transposition of the oncogene c-ets-1 in a t(11; 19) (q 23; p 13) cell line transient during clonal evolution of blast crisis chronic myeloid leukemia

Leukemia, 1988-02, Vol.2 (2), p.74-78

1988

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Localization of the SRC oncogene to chromosome band 20q11.2 and loss of this gene with deletion (20q) in two leukemic patients

Blood, 1989-10, Vol.74 (5), p.1768-1773

1989

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Evidence for the repeated primary non-disjunction of chromosome 21 as a result of premature centromere division (PCD)

Human genetics, 1986, Vol.72 (1), p.58-62

1986

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An enzymatic method for erythrocyte acetylcholinesterase

Clinical chemistry (Baltimore, Md.), 1988-06, Vol.34 (6), p.1055-1057

1988

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Ph‐negative chronic myeloid leukaemia

British journal of haematology, 1987-07, Vol.66 (3), p.311-314

1987

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A mechanism of x chromosome aneuploidy in lymphocytes of aging women

Human genetics, 1975-06, Vol.28 (2), p.153-158

Fitzgerald, P H

1975

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Assignments of polymorphic loci on chromosome 13 refined by in situ hybridization

Genomics (San Diego, Calif.), 1992-04, Vol.12 (4), p.852-853

1992

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Basophils exhibit rearrangement of the bcr gene in Philadelphia chromosome-positive chronic myeloid leukemia

Leukemia, 1988-03, Vol.2 (3), p.141-143

1988

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Acquired Homozygosity of the Rearranged bcr Allele During the Acute Leukemic Phase of a Patient With Ph-Negative Chronic Myeloid Leukemia

Blood, 1988-07, Vol.72 (1), p.24-28

1988

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Trisomy 18 mosaicism with complete peripheral lymphocyte trisomy and normal intelligence

Clinical genetics, 1992-01, Vol.41 (1), p.36-38

1992

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A sequence homologous to kappa-deleting element is located 5' to the human JK locus

Nucleic acids research, 1989-01, Vol.17 (2), p.809-809

1989

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Sustained complete remission in Richter's syndrome

Cancer, 1987-03, Vol.59 (5), p.1036-1039

1987

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Sex chromosome loss and clones characterized by autosomal abnormality in cultured corneal fibroblasts of man

Cytogenetic and genome research, 1984, Vol.38 (1), p.29-33

1984

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Involvement of immunoglobulin heavy- and light-chain (kappa) gene clusters in a human B-cell translocation, t(2;14)

Cytogenetic and genome research, 1989, Vol.52 (1-2), p.50-56

1989

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Basophils (Bsp-1+) Derive From the Leukemic Clone in Human Myeloid Leukemias Involving the Chromosome Breakpoint 9q34

Blood, 1989-02, Vol.73 (3), p.777-781

1989

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Nucleolar silver-staining patterns related to cell cycle phase and cell generation of PHA-stimulated human lymphocytes

Cytobios, 1984, Vol.41 (161), p.23

1984

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Carotid Stump Syndrome: Outcome from Surgical Management

Mosaicism with a normal cell line and an autosomal structural rearrangement

DNA sequence analysis of the major breakpoint cluster region of the BCR gene rearranged in Philadelphia-positive human leukemias

Genomic diversity correlates with clinical variation in Ph′-negative chronic myeloid leukaemia

Essential thrombocythaemia and the Philadelphia chromosome

Localization of the TRK proto-oncogene to human chromosome bands 1q23-1q24

Telomeric association of chromosomes in B-cell lymphoid leukemia

Effect of daylight on the reaction of thiols with Ellman's reagent, 5,5'-dithiobis(2-nitrobenzoic acid)

A Monoclonal Antibody Reacting With Human Basophils

Transposition of the oncogene c-ets-1 in a t(11; 19) (q 23; p 13) cell line transient during clonal evolution of blast crisis chronic myeloid leukemia

Localization of the SRC oncogene to chromosome band 20q11.2 and loss of this gene with deletion (20q) in two leukemic patients

Evidence for the repeated primary non-disjunction of chromosome 21 as a result of premature centromere division (PCD)

An enzymatic method for erythrocyte acetylcholinesterase

Ph‐negative chronic myeloid leukaemia

A mechanism of x chromosome aneuploidy in lymphocytes of aging women

Assignments of polymorphic loci on chromosome 13 refined by in situ hybridization

Basophils exhibit rearrangement of the bcr gene in Philadelphia chromosome-positive chronic myeloid leukemia

Acquired Homozygosity of the Rearranged bcr Allele During the Acute Leukemic Phase of a Patient With Ph-Negative Chronic Myeloid Leukemia

Trisomy 18 mosaicism with complete peripheral lymphocyte trisomy and normal intelligence

A sequence homologous to kappa-deleting element is located 5' to the human JK locus

Sustained complete remission in Richter's syndrome

Sex chromosome loss and clones characterized by autosomal abnormality in cultured corneal fibroblasts of man

Involvement of immunoglobulin heavy- and light-chain (kappa) gene clusters in a human B-cell translocation, t(2;14)

Basophils (Bsp-1+) Derive From the Leukemic Clone in Human Myeloid Leukemias Involving the Chromosome Breakpoint 9q34

Nucleolar silver-staining patterns related to cell cycle phase and cell generation of PHA-stimulated human lymphocytes

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