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Clonally-Related Composite Classic Hodgkin Lymphoma and Follicular Lymphoma

American journal of clinical pathology, 2021-10, Vol.156 (Supplement_1), p.S100-S101

2021

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The rates of G:C→T:A and G:C→C:G transversions at CpG dinucleotides in the human factor IX gene

American journal of human genetics, 1994-05, Vol.54 (5), p.831-835

1994

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Erratum: Mayo prognostic model for WHO-defined chronic myelomonocytic leukemia: ASXL1 and spliceosome component mutations and outcomes

Leukemia, 2013-10, Vol.27 (10), p.2112-2112

2013

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Hemophilia B in a male with a four-base insertion that arose in the germline of his mother

Nucleic acids research, 1989-12, Vol.17 (23), p.10139-10139

1989

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Erratum: Molecular correlates of anemia in primary myelofibrosis: a significant and independent association with U2AF1 mutations

Blood cancer journal (New York), 2016-05, Vol.6 (5), p.e416-e416

2016

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Mutations at arginine residues in two Asian hemophilia B patients

Nucleic acids research, 1990-04, Vol.18 (7), p.1924-1924

1990

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Are some apparently simple deletions actually two concerted deletions that result from interacting RY(i) hairpin loops?

American journal of human genetics, 1995-01, Vol.56 (1), p.343-346

1995

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Evidence that descendants of three founders constitute about 25% of hemophilia B in the united states

Genomics (San Diego, Calif.), 1991-08, Vol.10 (4), p.1093-1096

1991

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Survival trends in primary myelodysplastic syndromes: a comparative analysis of 1000 patients by year of diagnosis and treatment

Blood cancer journal (New York), 2016-04, Vol.6, p.e414

2016

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Erratum: Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome

Blood cancer journal (New York), 2015-02, Vol.5 (2), p.e280-e280

2015

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Why does the human factor IX gene have a G + C content of 40% ?

American journal of human genetics, 1991-10, Vol.49 (4), p.839-850

1991

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A randomized trial of anthracycline dose intensification during induction of younger patients with acute myeloid leukemia: Results of Eastern Cooperative Oncology Group study E1900

Journal of clinical oncology, 2009-05, Vol.27 (15_suppl), p.7003-7003

2009

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Microdeletions in the factor IX gene: three recurrences associated with a quasipalindromic sequence

Human molecular genetics, 1994-01, Vol.3 (1), p.191-192

1994

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DUSP22 AND TP63 REARRANGEMENTS PREDICT OUTCOME OF ALK‐NEGATIVE ANAPLASTIC LARGE CELL LYMPHOMA: A DANISH COHORT STUDY

Hematological oncology, 2017-06, Vol.35 (S2), p.391-392

2017

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A mutation in the 3' untranslated region of the factor IX gene in four families with hemophilia B

Human molecular genetics, 1993-08, Vol.2 (8), p.1309-1310

1993

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Two novel factor IX promoter mutations: incremental progress towards ‘saturation in vivo mutagenesis’ of a human promoter region

Human molecular genetics, 1995-04, Vol.4 (4), p.769-770

1995

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Clinical correlates of JAK2V617F allele burden in essential thrombocythemia

Journal of clinical oncology, 2007-06, Vol.25 (18_suppl), p.7030-7030

2007

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Chronic Lymphocytic Leukemia With t(2; 14)(p16; q32) Involves the BCL11A and IgH Genes and Is Associated With Atypical Morphologic Features and Unmutated IgV sub(H) Genes

American journal of clinical pathology, 2009-05, Vol.131 (5)

2009

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Cytogenetic analysis using multiple myeloma targets in POEMS syndrome

Journal of clinical oncology, 2007-06, Vol.25 (18_suppl), p.8116-8116

2007

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Abstract PD10-02: Round-Robin Review of HER2 Testing in the Context of Adjuvant Therapy for Breast Cancer (NCCTG N9831/BCIRG006/BCIRG005)

Cancer research (Chicago, Ill.), 2010-12, Vol.70 (24_Supplement), p.PD10-02-PD10-02

2010

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Histologic and Immunohistochemical Study of Bone Marrow Monocytic Nodules in 21 Cases With Myelodysplasia

American journal of clinical pathology, 2004-03, Vol.121 (3), p.874-881

2004

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Reported In Vivo Splice-Site Mutations in the Factor IX Gene: Severity of Splicing Defects and a Hypothesis for Predicting Deleterious Splice Donor Mutations

Human mutation, 1999-01, Vol.13 (3), p.221-231

1999

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The rates of G:C arrow right T:A and G:C arrow right C:G transversions at CpG dinucleotides in the human factor IX gene

American journal of human genetics, 1994-01, Vol.54 (5), p.831-835

1994

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PRE : a novel element with the hallmarks of a retrotransporon derived from an unknown structural RNA

Nucleic acids research, 1992, Vol.20 (19)

1992

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The pattern of spontaneous germ-line mutation: Relative rates of mutation at or near CpG dinucleotides in the factor IC gene

Human genetics, 1993-01, Vol.91 (5), p.496-503

1993

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Clonally-Related Composite Classic Hodgkin Lymphoma and Follicular Lymphoma

The rates of G:C→T:A and G:C→C:G transversions at CpG dinucleotides in the human factor IX gene

Erratum: Mayo prognostic model for WHO-defined chronic myelomonocytic leukemia: ASXL1 and spliceosome component mutations and outcomes

Hemophilia B in a male with a four-base insertion that arose in the germline of his mother

Erratum: Molecular correlates of anemia in primary myelofibrosis: a significant and independent association with U2AF1 mutations

Mutations at arginine residues in two Asian hemophilia B patients

Are some apparently simple deletions actually two concerted deletions that result from interacting RY(i) hairpin loops?

Evidence that descendants of three founders constitute about 25% of hemophilia B in the united states

Survival trends in primary myelodysplastic syndromes: a comparative analysis of 1000 patients by year of diagnosis and treatment

Erratum: Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome

Why does the human factor IX gene have a G + C content of 40% ?

A randomized trial of anthracycline dose intensification during induction of younger patients with acute myeloid leukemia: Results of Eastern Cooperative Oncology Group study E1900

Microdeletions in the factor IX gene: three recurrences associated with a quasipalindromic sequence

DUSP22 AND TP63 REARRANGEMENTS PREDICT OUTCOME OF ALK‐NEGATIVE ANAPLASTIC LARGE CELL LYMPHOMA: A DANISH COHORT STUDY

A mutation in the 3' untranslated region of the factor IX gene in four families with hemophilia B

Two novel factor IX promoter mutations: incremental progress towards ‘saturation in vivo mutagenesis’ of a human promoter region

Clinical correlates of JAK2V617F allele burden in essential thrombocythemia

Chronic Lymphocytic Leukemia With t(2; 14)(p16; q32) Involves the BCL11A and IgH Genes and Is Associated With Atypical Morphologic Features and Unmutated IgV sub(H) Genes

Cytogenetic analysis using multiple myeloma targets in POEMS syndrome

Abstract PD10-02: Round-Robin Review of HER2 Testing in the Context of Adjuvant Therapy for Breast Cancer (NCCTG N9831/BCIRG006/BCIRG005)

Histologic and Immunohistochemical Study of Bone Marrow Monocytic Nodules in 21 Cases With Myelodysplasia

Reported In Vivo Splice-Site Mutations in the Factor IX Gene: Severity of Splicing Defects and a Hypothesis for Predicting Deleterious Splice Donor Mutations

The rates of G:C arrow right T:A and G:C arrow right C:G transversions at CpG dinucleotides in the human factor IX gene

PRE : a novel element with the hallmarks of a retrotransporon derived from an unknown structural RNA

The pattern of spontaneous germ-line mutation: Relative rates of mutation at or near CpG dinucleotides in the factor IC gene

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