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Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells

Human molecular genetics, 1994-07, Vol.3 (7), p.1035-1039

1994

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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 factor IX gene as a model for analysis of human germline mutations: an update

Human molecular genetics, 1996-01, Vol.5 (Supplement-1), p.1505-1514

1996

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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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The rates and patterns of deletions in the human factor IX gene

American journal of human genetics, 1994-02, Vol.54 (2), p.201-213

1994

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Germ-line origins of mutation in families with hemophilia B : the sex ratio varies with the type of mutation

American journal of human genetics, 1993, Vol.52 (1), p.152-166

1993

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Germline mosaicism in a female who seemed to be a carrier by sequence analysis

Human molecular genetics, 1995-11, Vol.4 (11), p.2181-2182

1995

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Translocation t(11;14) and survival of patients with light chain (AL) amyloidosis

Haematologica (Roma), 2009-03, Vol.94 (3), p.380-386

2009

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Molecular epidemiology of factor IX germline mutations in Mexican Hispanics: pattern of mutation and potential founder effects

Thrombosis and haemostasis, 1995-12, Vol.74 (6), p.1416

1995

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The pattern of factor IX germ-line mutation in Asians is similar to that of Caucasians

American journal of human genetics, 1990-11, Vol.47 (5), p.835-841

1990

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FIP1L1-PDGFRA fusion: prevalence and clinicopathologic correlates in 89 consecutive patients with moderate to severe eosinophilia

Blood, 2004-11, Vol.104 (10), p.3038-3045

2004

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CHIC2 deletion, a surrogate for FIP1L1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate therapy

Blood, 2003-11, Vol.102 (9), p.3093-3096

2003

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Germline mutations in the factor IX gene: a comparison of the pattern in Caucasians and non-Caucasians

Human molecular genetics, 1993-03, Vol.2 (3), p.293-298

1993

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Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients

American journal of human genetics, 2003-11, Vol.73 (5), p.1027-1040

2003

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Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human gene

American journal of human genetics, 1990-08, Vol.47 (2), p.202-217

1990

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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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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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Missense mutations and evolutionary conservation of amino acids: evidence that many of the amino acids in factor IX function as "spacer" elements

American journal of human genetics, 1991-10, Vol.49 (4), p.820-838

1991

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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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Analysis of intratumoral heterogeneity and amplification status in breast carcinomas with equivocal (2+) HER-2 immunostaining

American journal of clinical pathology, 2005-08, Vol.124 (2), p.273-281

2005

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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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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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Factor VIII gene inversions causing severe hemophilia A originate almost exclusively in male germ cells

Clonally-Related Composite Classic Hodgkin Lymphoma and Follicular Lymphoma

The factor IX gene as a model for analysis of human germline mutations: an update

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

The rates and patterns of deletions in the human factor IX gene

Germ-line origins of mutation in families with hemophilia B : the sex ratio varies with the type of mutation

Germline mosaicism in a female who seemed to be a carrier by sequence analysis

Translocation t(11;14) and survival of patients with light chain (AL) amyloidosis

Molecular epidemiology of factor IX germline mutations in Mexican Hispanics: pattern of mutation and potential founder effects

The pattern of factor IX germ-line mutation in Asians is similar to that of Caucasians

FIP1L1-PDGFRA fusion: prevalence and clinicopathologic correlates in 89 consecutive patients with moderate to severe eosinophilia

CHIC2 deletion, a surrogate for FIP1L1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate therapy

Germline mutations in the factor IX gene: a comparison of the pattern in Caucasians and non-Caucasians

Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients

Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human gene

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

Mutations at arginine residues in two Asian hemophilia B patients

Missense mutations and evolutionary conservation of amino acids: evidence that many of the amino acids in factor IX function as "spacer" elements

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

Analysis of intratumoral heterogeneity and amplification status in breast carcinomas with equivocal (2+) HER-2 immunostaining

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

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

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