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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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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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Familial endometrial cancer in female carriers of MSH6 germline mutations

Nature genetics, 1999-10, Vol.23 (2), p.142-144

1999

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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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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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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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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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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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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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Misleading variant chromosome 12 in prenatal diagnosis

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

2006

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Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients

The Journal of pathology, 2000-11, Vol.192 (3), p.328-335

2000

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Conventional and Tissue Microarray Immunohistochemical Expression Analysis of Mismatch Repair in Hereditary Colorectal Tumors

The American journal of pathology, 2003-02, Vol.162 (2), p.469-477

2003

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Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene

Genes chromosomes & cancer, 2001-07, Vol.31 (3), p.274-281

2001

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Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer

The New England journal of medicine, 1998-08, Vol.339 (8), p.511-518

1998

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Genotype assignment of haemophilia A by use of intragenic and extragenic restriction fragment length polymorphisms

Thrombosis and haemostasis, 1987-04, Vol.57 (2), p.131-136

1987

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A near false-negative finding of mosaic trisomy 21-a cautionary tale

Prenatal diagnosis, 1998-07, Vol.18 (7), p.742-746

1998

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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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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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The common sense model of self-regulation and psychological adjustment to predictive genetic testing: a prospective study

Psycho-oncology (Chichester, England), 2007-12, Vol.16 (12), p.1121-1129

2007

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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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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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Physical condition, longevity, and social performance of Dutch haemophiliacs, 1972-85

BMJ, 1989-01, Vol.298 (6668), p.235-238

1989

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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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Bias in detection of instability of the (C)8 mononucleotide repeat of MSH6 in tumours from HNPCC patients

Oncogene, 2001-09, Vol.20 (43), p.6241-6244

2001

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

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

Familial endometrial cancer in female carriers of MSH6 germline mutations

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

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

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

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

Identification of HNPCC by molecular analysis of colorectal and endometrial tumors

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

Misleading variant chromosome 12 in prenatal diagnosis

Prediction of a mismatch repair gene defect by microsatellite instability and immunohistochemical analysis in endometrial tumours from HNPCC patients

Conventional and Tissue Microarray Immunohistochemical Expression Analysis of Mismatch Repair in Hereditary Colorectal Tumors

Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene

Clinical Findings with Implications for Genetic Testing in Families with Clustering of Colorectal Cancer

Genotype assignment of haemophilia A by use of intragenic and extragenic restriction fragment length polymorphisms

A near false-negative finding of mosaic trisomy 21-a cautionary tale

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

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

The common sense model of self-regulation and psychological adjustment to predictive genetic testing: a prospective study

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

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

Physical condition, longevity, and social performance of Dutch haemophiliacs, 1972-85

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

Bias in detection of instability of the (C)8 mononucleotide repeat of MSH6 in tumours from HNPCC patients

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

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