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Shared Genetic Susceptibility to Breast Cancer, Brain Tumors, and Fanconi Anemia

JNCI : Journal of the National Cancer Institute, 2003-10, Vol.95 (20), p.1548-1551

2003

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Recommendations for locus-specific databases and their curation

Human mutation, 2008, Vol.29 (1), p.2-5

2008

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Fanconi anemia diagnosis and the diepoxybutane (DEB) test

Experimental hematology, 1993-06, Vol.21 (6), p.731

Auerbach, A D

1993

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Use and outcomes of venous thromboembolism prophylaxis after spinal fusion surgery

Journal of thrombosis and haemostasis, 2011-07, Vol.9 (7), p.1318-1325

2011

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Haematopoietic cell transplantation in patients with Fanconi anaemia using alternate donors: results of a total body irradiation dose escalation trial

British journal of haematology, 2000-04, Vol.109 (1), p.121-129

2000

Volltextzugriff (PDF)

Bone marrow transplantation for Fanconi anemia

Blood, 1995-10, Vol.86 (7), p.2856-2862

1995

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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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Hematopoietic reconstitution in a patient with Fanconi's anemia by means of umbilical-cord blood from an HLA-identical sibling

The New England journal of medicine, 1989-10, Vol.321 (17), p.1174

1989

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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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Fanconi anaemia group A (FANCA) mutations in Israeli non-Ashkenazi Jewish patients

British journal of haematology, 2000-10, Vol.111 (1), p.338-343

2000

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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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International Fanconi Anemia Registry: Relation of Clinical Symptoms to Diepoxybutane Sensitivity

Blood, 1989-02, Vol.73 (2), p.391-396

1989

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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

Volltextzugriff (PDF)

Harms associated with single unit perioperative transfusion: retrospective population based analysis

BMJ (Online), 2015-06, Vol.350, p.h3037

2015

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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

Volltextzugriff (PDF)

Unrelated donor bone marrow transplantation for Fanconi anemia

Bone marrow transplantation (Basingstoke), 1996, Vol.17 (1), p.43-47

1996

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3

British journal of cancer, 1999-03, Vol.79 (7-8), p.1049-1052

1999

Volltextzugriff (PDF)

Fanconi anemia and moyamoya: evidence for an association

Neurology, 1995-05, Vol.45 (5), p.998

1995

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Fanconi Anemia

Dermatologic clinics, 1995-01, Vol.13 (1), p.41-49

Auerbach, Arleen D.

1995

Volltextzugriff (PDF)

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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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

Volltextzugriff (PDF)

structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases

Human mutation, 2007-10, Vol.28 (10), p.931-932

2007

Volltextzugriff (PDF)

The Genomic Organization of the Fanconi Anemia Group A (FAA) Gene

Genomics (San Diego, Calif.), 1997-05, Vol.41 (3), p.309-314

1997

Volltextzugriff (PDF)

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Shared Genetic Susceptibility to Breast Cancer, Brain Tumors, and Fanconi Anemia

Recommendations for locus-specific databases and their curation

Fanconi anemia diagnosis and the diepoxybutane (DEB) test

Use and outcomes of venous thromboembolism prophylaxis after spinal fusion surgery

Haematopoietic cell transplantation in patients with Fanconi anaemia using alternate donors: results of a total body irradiation dose escalation trial

Bone marrow transplantation for Fanconi anemia

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

Hematopoietic reconstitution in a patient with Fanconi's anemia by means of umbilical-cord blood from an HLA-identical sibling

Mutation analysis of the Fanconi anemia gene FACC

Fanconi anaemia group A (FANCA) mutations in Israeli non-Ashkenazi Jewish patients

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

International Fanconi Anemia Registry: Relation of Clinical Symptoms to Diepoxybutane Sensitivity

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

Harms associated with single unit perioperative transfusion: retrospective population based analysis

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

Unrelated donor bone marrow transplantation for Fanconi anemia

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

Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3

Fanconi anemia and moyamoya: evidence for an association

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

Fanconi Anemia

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

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

structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases

The Genomic Organization of the Fanconi Anemia Group A (FAA) Gene

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