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Morphologic and cytogenetic variables affect the flow cytometric recovery of plasma cell myeloma cells in bone marrow aspirates

International journal of laboratory hematology, 2015-12, Vol.37 (6), p.797-808

2015

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The Human PECAM1 Gene Maps to 17q23

Genomics (San Diego, Calif.), 1996-06, Vol.34 (2), p.229-232

1996

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Human hepatic lipase. Cloned cDNA sequence, restriction fragment length polymorphisms, chromosomal localization, and evolutionary relationships with lipoprotein lipase and pancreatic lipase

The Journal of biological chemistry, 1988-01, Vol.263 (3), p.1107-1110

1988

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Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome

American journal of human genetics, 1988-11, Vol.43 (5), p.587-596

1988

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Chromosome 17 Deletions and p53 Gene Mutations in Colorectal Carcinomas

Science (American Association for the Advancement of Science), 1989-04, Vol.244 (4901), p.217-221

1989

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Molecular Dissection of a Contiguous Gene Syndrome: Frequent Submicroscopic Deletions, Evolutionarily Conserved Sequences, and a Hypomethylated "Island" in the Miller-Dieker Chromosome Region

Proceedings of the National Academy of Sciences - PNAS, 1989-07, Vol.86 (13), p.5136-5140

1989

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Isolation of cDNA Clones for the Catalytic γ Subunit of Mouse Muscle Phosphorylase Kinase: Expression of mRNA in Normal and Mutant Phk Mice

Proceedings of the National Academy of Sciences - PNAS, 1987-05, Vol.84 (9), p.2886-2890

1987

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Salvage Immunotherapy Using Donor Leukocyte Infusions as Treatment for Relapsed Chronic Myelogenous Leukemia After Allogeneic Bone Marrow Transplantation: Efficacy and Toxicity of a Defined T-Cell Dose

Blood, 1993-10, Vol.82 (8), p.2310-2318

1993

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Molecular Cloning and Chromosomal Localization of Human 4-β -galactosyltransferase

Proceedings of the National Academy of Sciences - PNAS, 1986-12, Vol.83 (23), p.8918-8922

1986

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Structural analysis of a hepatitis B virus genome integrated into chromosome 17p of a human hepatocellular carcinoma

Journal of Virology, 1988-11, Vol.62 (11), p.4224-4231

1988

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Mantle Cell Lymphoma in Lymph Nodes with Metastatic Small Cell Carcinoma of Lung: A Diagnostic and Treatment Dilemma

Leukemia & lymphoma, 2004-02, Vol.45 (2), p.409-414

2004

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The human apolipoprotein B-100 gene: A highly polymorphic gene that maps to the short arm of chromosome 2

Biochemical and biophysical research communications, 1985-11, Vol.133 (1), p.248-255

1985

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The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1

American journal of human genetics, 1986-04, Vol.38 (4), p.437-446

1986

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An anonymous single-copy clone, pC63, from chromosome 17q23-qter identifies a frequent RFLP [HGM9 no. D17S21]

Nucleic acids research, 1987-11, Vol.15 (21), p.9096-9096

1987

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Cosmid 1-26 defines four RFLPs on chromosome 17q23-qter [HGM9 no. D17S20]

Nucleic acids research, 1987-11, Vol.15 (21), p.9097-9097

1987

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Molecular cloning and characterization of a cDNA for human granulocyte colony-stimulating factor (G-CSF) from a glioblastoma multiforme cell line and localization of the G-CSF gene to chromosome band 17q21

Oncogene research, 1987-08, Vol.1 (3), p.209

1987

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637 The human multimerin gene maps to chromosome 4q22

Journal of pediatric hematology/oncology, 1998-07, Vol.20 (4), p.386

1998

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Molecular characterization of human and bovine rod photoreceptor cGMP phosphodiesterase α-subunit and chromosomal localization of the human gene

Genomics (San Diego, Calif.), 1990-02, Vol.6 (2), p.272-283

1990

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Construction of a YAC contig encompassing the Usher syndrome type 1C and familial hyperinsulinism loci on chromosome 11p14-15.1

Genome research, 1996-06, Vol.6 (6), p.504-514

1996

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Alteration and Abnormal Expression of the c-myc Oncogene in Human Multiple Myeloma

Blood, 1988-01, Vol.71 (1), p.30-35

1988

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Mapping of human methylmalonyl CoA mutase (MUT) locus on chromosome 6

American journal of human genetics, 1988-06, Vol.42 (6), p.839-846

1988

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Localization of the human thyroxine-binding globulin gene to the long arm of the X chromosome (Xq21-22)

American journal of human genetics, 1987-09, Vol.41 (3), p.428-435

1987

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A Myeloid-Related Sequence That Localizes to Human Chromosome 8q21.1-22

Blood, 1988-06, Vol.71 (6), p.1713-1719

1988

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A myeloid-related sequence that localizes to human chromosome 8q21.1-22

Blood, 1988-06, Vol.71 (6), p.1713-1719

1988

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Highly polymorphic locus D15S24 (CMW-1) maps to 15pter-q13. [HGM9 provisional no. D15S24]

Nucleic acids research, 1988-09, Vol.16 (17), p.8740-8740

1988

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Morphologic and cytogenetic variables affect the flow cytometric recovery of plasma cell myeloma cells in bone marrow aspirates

The Human PECAM1 Gene Maps to 17q23

Human hepatic lipase. Cloned cDNA sequence, restriction fragment length polymorphisms, chromosomal localization, and evolutionary relationships with lipoprotein lipase and pancreatic lipase

Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome

Chromosome 17 Deletions and p53 Gene Mutations in Colorectal Carcinomas

Molecular Dissection of a Contiguous Gene Syndrome: Frequent Submicroscopic Deletions, Evolutionarily Conserved Sequences, and a Hypomethylated "Island" in the Miller-Dieker Chromosome Region

Isolation of cDNA Clones for the Catalytic γ Subunit of Mouse Muscle Phosphorylase Kinase: Expression of mRNA in Normal and Mutant Phk Mice

Salvage Immunotherapy Using Donor Leukocyte Infusions as Treatment for Relapsed Chronic Myelogenous Leukemia After Allogeneic Bone Marrow Transplantation: Efficacy and Toxicity of a Defined T-Cell Dose

Molecular Cloning and Chromosomal Localization of Human 4-β -galactosyltransferase

Structural analysis of a hepatitis B virus genome integrated into chromosome 17p of a human hepatocellular carcinoma

Mantle Cell Lymphoma in Lymph Nodes with Metastatic Small Cell Carcinoma of Lung: A Diagnostic and Treatment Dilemma

The human apolipoprotein B-100 gene: A highly polymorphic gene that maps to the short arm of chromosome 2

The anonymous polymorphic DNA clone D1S1, previously mapped to human chromosome 1p36 by in situ hybridization, is from chromosome 3 and is duplicated on chromosome 1

An anonymous single-copy clone, pC63, from chromosome 17q23-qter identifies a frequent RFLP [HGM9 no. D17S21]

Cosmid 1-26 defines four RFLPs on chromosome 17q23-qter [HGM9 no. D17S20]

Molecular cloning and characterization of a cDNA for human granulocyte colony-stimulating factor (G-CSF) from a glioblastoma multiforme cell line and localization of the G-CSF gene to chromosome band 17q21

637 The human multimerin gene maps to chromosome 4q22

Molecular characterization of human and bovine rod photoreceptor cGMP phosphodiesterase α-subunit and chromosomal localization of the human gene

Construction of a YAC contig encompassing the Usher syndrome type 1C and familial hyperinsulinism loci on chromosome 11p14-15.1

Alteration and Abnormal Expression of the c-myc Oncogene in Human Multiple Myeloma

Mapping of human methylmalonyl CoA mutase (MUT) locus on chromosome 6

Localization of the human thyroxine-binding globulin gene to the long arm of the X chromosome (Xq21-22)

A Myeloid-Related Sequence That Localizes to Human Chromosome 8q21.1-22

A myeloid-related sequence that localizes to human chromosome 8q21.1-22

Highly polymorphic locus D15S24 (CMW-1) maps to 15pter-q13. [HGM9 provisional no. D15S24]

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