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Somatic Mosaicism in Fanconi Anemia: Evidence of Genotypic Reversion in Lymphohematopoietic Stem Cells

Proceedings of the National Academy of Sciences - PNAS, 2001-02, Vol.98 (5), p.2532-2537

2001

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Evaluation of growth and hormonal status in patients referred to the International Fanconi Anemia Registry

Pediatrics (Evanston), 2001-04, Vol.107 (4), p.744

2001

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Phenotypic correction of primary Fanconi anemia T cells with retroviral vectors as a diagnostic tool

Experimental hematology, 2002-05, Vol.30 (5), p.410-420

2002

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Sequence Variation in the Fanconi Anemia Gene FAA

Proceedings of the National Academy of Sciences - PNAS, 1997-11, Vol.94 (24), p.13051-13056

1997

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Phenotypic consequences of mutations in the Fanconi anemia FAC gene : An International Fanconi Anemia Registry study

Blood, 1997-07, Vol.90 (1), p.105-110

1997

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The need for more accurate and timely diagnosis in Fanconi anemia: a report from the International Fanconi Anemia Registry

Pediatrics (Evanston), 1993-06, Vol.91 (6), p.1116

1993

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Hematologic abnormalities in Fanconi anemia: an International Fanconi Anemia Registry study [see comments]

Blood, 1994-09, Vol.84 (5), p.1650-1655

1994

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Identification of Cytosolic Proteins That Bind to the Fanconi Anemia Complementation Group C Polypeptide in Vitro

The Journal of biological chemistry, 1995-04, Vol.270 (17), p.9876-9882

1995

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Mutation analysis of the Fanconi anemia gene FACC

American journal of human genetics, 1994-04, Vol.54 (4), p.595-601

1994

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Carrier Frequency of the IVS4 + 4 A → T Mutation of the Fanconi Anemia Gene FAC in the Ashkenazi Jewish Population

Blood, 1995-12, Vol.86 (11), p.4034-4038

1995

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Disorders of DNA replication and repair

Current opinion in pediatrics, 1997-12, Vol.9 (6), p.600-616

1997

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The PISSLRE gene : Structure, exon skipping, and exclusion as tumor suppressor in breast cancer

Genomics (San Diego, Calif.), 1999-02, Vol.56 (1), p.90-97

1999

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Identification of cytosolic proteins that bind to the Fanconi anemia complementation group C polypeptide in vitro. Evidence for a multimeric complex

The Journal of biological chemistry, 1995-04, Vol.270 (17), p.9876-9882

1995

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Diagnosis of Fanconi anemia in patients without congenital malformations: An international Fanconi anemia registry study

American journal of medical genetics, 1997-01, Vol.68 (1), p.58-61

1997

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A locus for Fanconi anemia on 16q determined by homozygosity mapping

American journal of human genetics, 1996-08, Vol.59 (2), p.377-384

1996

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Phenotypic Consequences of Mutations in the Fanconi Anemia FAC Gene: An International Fanconi Anemia Registry Study

Blood, 1997-07, Vol.90 (1), p.105-110

1997

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Hematologic Abnormalities in Fanconi Anemia: An International Fanconi Anemia Registry Study

Blood, 1994-09, Vol.84 (5), p.1650-1655

1994

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New molecular diagnostic tests for two congenital forms of anemia

Journal of clinical laboratory analysis, 1997, Vol.11 (1), p.17-22

1997

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ThePISSLREGene: Structure, Exon Skipping, and Exclusion as Tumor Suppressor in Breast Cancer

Genomics (San Diego, Calif.), 1999-02, Vol.56 (1), p.90-97

1999

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9 - Detection of Horseradish Peroxidase by Colorimetry

Nonisotopic Probing, Blotting, and Sequencing, 1995, p.217,I-236,II

Verlander, Peter C.

Second Edition, 1995

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8 - Detection of Horseradish Peroxidase by Colorimetry

Nonisotopic DNA Probe Techniques, 1992, p.185,198a,198b,199-198,198a,198b,201

Verlander, Peter C.

1992

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Epidermal Growth Factor Receptor Mutation Testing in the Care of Lung Cancer Patients

Clinical cancer research, 2006-07, Vol.12 (14), p.4403s-4408s

2006

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Characterization and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer

Genomics (San Diego, Calif.), 1998-09, Vol.52 (3), p.325-331

1998

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Characterization and Screening for Mutations of the Growth Arrest-Specific 11 (GAS11) andC16orf3Genes at 16q24.3 in Breast Cancer

Genomics (San Diego, Calif.), 1998-09, Vol.52 (3), p.325-331

1998

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Molecular Sequence Data
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Anemias. Hemoglobinopathies
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Somatic Mosaicism in Fanconi Anemia: Evidence of Genotypic Reversion in Lymphohematopoietic Stem Cells

Evaluation of growth and hormonal status in patients referred to the International Fanconi Anemia Registry

Positional cloning of the Fanconi anaemia group A gene

Phenotypic correction of primary Fanconi anemia T cells with retroviral vectors as a diagnostic tool

Sequence Variation in the Fanconi Anemia Gene FAA

Phenotypic consequences of mutations in the Fanconi anemia FAC gene : An International Fanconi Anemia Registry study

The need for more accurate and timely diagnosis in Fanconi anemia: a report from the International Fanconi Anemia Registry

Hematologic abnormalities in Fanconi anemia: an International Fanconi Anemia Registry study [see comments]

Identification of Cytosolic Proteins That Bind to the Fanconi Anemia Complementation Group C Polypeptide in Vitro

Mutation analysis of the Fanconi anemia gene FACC

Carrier Frequency of the IVS4 + 4 A → T Mutation of the Fanconi Anemia Gene FAC in the Ashkenazi Jewish Population

Disorders of DNA replication and repair

The PISSLRE gene : Structure, exon skipping, and exclusion as tumor suppressor in breast cancer

Identification of cytosolic proteins that bind to the Fanconi anemia complementation group C polypeptide in vitro. Evidence for a multimeric complex

Diagnosis of Fanconi anemia in patients without congenital malformations: An international Fanconi anemia registry study

A locus for Fanconi anemia on 16q determined by homozygosity mapping

Phenotypic Consequences of Mutations in the Fanconi Anemia FAC Gene: An International Fanconi Anemia Registry Study

Hematologic Abnormalities in Fanconi Anemia: An International Fanconi Anemia Registry Study

New molecular diagnostic tests for two congenital forms of anemia

ThePISSLREGene: Structure, Exon Skipping, and Exclusion as Tumor Suppressor in Breast Cancer

9 - Detection of Horseradish Peroxidase by Colorimetry

8 - Detection of Horseradish Peroxidase by Colorimetry

Epidermal Growth Factor Receptor Mutation Testing in the Care of Lung Cancer Patients

Characterization and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer

Characterization and Screening for Mutations of the Growth Arrest-Specific 11 (GAS11) andC16orf3Genes at 16q24.3 in Breast Cancer

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