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Experience of parental cancer in childhood is a risk factor for psychological distress during genetic cancer susceptibility testing

Annals of oncology, 2006-07, Vol.17 (7), p.1090-1095

2006

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Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study

Clinical genetics, 2007-01, Vol.71 (1), p.35-42

2007

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Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas

European journal of endocrinology, 2005-01, Vol.152 (1), p.87-94

2005

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Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

Journal of medical genetics, 2001-05, Vol.38 (5), p.318-322

2001

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Misleading variant chromosome 12 in prenatal diagnosis

Prenatal diagnosis, 2006-06, Vol.26 (6), p.587-588

2006

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Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP)

Journal of medical genetics, 2005-09, Vol.42 (9), p.e54-e54

2005

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Identification of HNPCC by molecular analysis of colorectal and endometrial tumors

Disease markers, 2004, Vol.20 (4-5), p.207-213

2004

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The use of preventive health care services: Carrier testing for the genetic disorder haemophilia

Social science & medicine (1982), 1993-09, Vol.37 (5), p.639-648

1993

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Mortality and causes of death in Dutch haemophiliacs, 1973–86

British journal of haematology, 1989-01, Vol.71 (1), p.71-76

1989

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Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases

Familial cancer, 2003, Vol.2 (2), p.79-85

2003

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First trimester prenatal diagnosis of haemophilia A: Two years' experience

Prenatal diagnosis, 1988-07, Vol.8 (6), p.411-421

1988

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Unbalanced karyotype with normal phenotype in a family with translocation (8;13) (p21;q22)

Clinical genetics, 1985-05, Vol.27 (5), p.487-495

1985

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Sex ratio of the mutation frequencies in haemophilia A : estimation and meta-analysis

Human genetics, 1990-12, Vol.86 (2), p.139-146

1990

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The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B

Annals of hematology, 1992, Vol.64 (1), p.2-11

1992

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Carrier detection of haemophilia B by using an intragenic restriction-fragment length polymorphism

Thrombosis and haemostasis, 1985-01, Vol.54 (2), p.506-509

1985

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Modern haemophilia treatment: medical improvements and quality of life

Journal of internal medicine, 1990-12, Vol.228 (6), p.633-640

1990

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Somatic origin of inherited haemophilia A

Human genetics, 1990-08, Vol.85 (3), p.288-292

1990

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Diagnostic Approach and Management of Lynch Syndrome (Hereditary Nonpolyposis Colorectal Carcinoma): A Guide for Clinicians

CA: a cancer journal for clinicians, 2006-07, Vol.56 (4), p.213-225

2006

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Carrier testing and prenatal diagnosis for hemophilia: Experiences and attitudes of 549 potential and obligate carriers

American journal of medical genetics, 1990-09, Vol.37 (1), p.147-154

1990

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Bleeding in carriers of hemophilia

Blood, 2006-07, Vol.108 (1), p.52-56

2006

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Sex ratio of the mutation frequencies in haemophilia A: coagulation assays and RFLP analysis

Journal of medical genetics, 1991-10, Vol.28 (10), p.672-680

1991

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Microsatellite Instability, Immunohistochemistry, and Additional PMS2 Staining in Suspected Hereditary Nonpolyposis Colorectal Cancer

Clinical cancer research, 2004-02, Vol.10 (3), p.972-980

2004

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Monosomy 8p: an easily overlooked syndrome

Journal of medical genetics, 1986-04, Vol.23 (2), p.153-154

1986

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From gene to disease; from SDHD, a defect in the respiratory chain, to paragangliomas and pheochromocytomas

Nederlands tijdschrift voor geneeskunde, 2002-11, Vol.146 (46), p.2188

2002

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Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance

Gastroenterology (New York, N.Y. 1943), 2004-07, Vol.127 (1), p.17-25

2004

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Experience of parental cancer in childhood is a risk factor for psychological distress during genetic cancer susceptibility testing

Family system characteristics and psychological adjustment to cancer susceptibility genetic testing: a prospective study

Increased prevalence of catecholamine excess and phaeochromocytomas in a well-defined Dutch population with SDHD-linked head and neck paragangliomas

Atypical HNPCC owing to MSH6 germline mutations: analysis of a large Dutch pedigree

Misleading variant chromosome 12 in prenatal diagnosis

Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP)

Identification of HNPCC by molecular analysis of colorectal and endometrial tumors

The use of preventive health care services: Carrier testing for the genetic disorder haemophilia

Mortality and causes of death in Dutch haemophiliacs, 1973–86

Bannayan-Riley-Ruvalcaba syndrome: further delineation of the phenotype and management of PTEN mutation-positive cases

First trimester prenatal diagnosis of haemophilia A: Two years' experience

Unbalanced karyotype with normal phenotype in a family with translocation (8;13) (p21;q22)

Sex ratio of the mutation frequencies in haemophilia A : estimation and meta-analysis

The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B

Carrier detection of haemophilia B by using an intragenic restriction-fragment length polymorphism

Modern haemophilia treatment: medical improvements and quality of life

Somatic origin of inherited haemophilia A

Diagnostic Approach and Management of Lynch Syndrome (Hereditary Nonpolyposis Colorectal Carcinoma): A Guide for Clinicians

Carrier testing and prenatal diagnosis for hemophilia: Experiences and attitudes of 549 potential and obligate carriers

Bleeding in carriers of hemophilia

Sex ratio of the mutation frequencies in haemophilia A: coagulation assays and RFLP analysis

Microsatellite Instability, Immunohistochemistry, and Additional PMS2 Staining in Suspected Hereditary Nonpolyposis Colorectal Cancer

Monosomy 8p: an easily overlooked syndrome

From gene to disease; from SDHD, a defect in the respiratory chain, to paragangliomas and pheochromocytomas

Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillance

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