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Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy

Neurology, 2011-07, Vol.77 (1), p.62-66

2011

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Consecutive or non-consecutive recurrent miscarriage: is there any difference in carrier status?

Human reproduction (Oxford), 2010-06, Vol.25 (6), p.1411-1414

2010

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Clinical relevance of diagnosing structural chromosome abnormalities in couples with repeated miscarriage

Human reproduction (Oxford), 2004-04, Vol.19 (4), p.1013-1017

2004

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Mutations in the testis-specific NALP14 gene in men suffering from spermatogenic failure

Human reproduction (Oxford), 2006-12, Vol.21 (12), p.3178-3184

2006

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Genetic aspects of miscarriage

Bailliere's best practice & research. Clinical obstetrics & gynaecology, 2000-10, Vol.14 (5), p.855-865

2000

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Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in the Netherlands: a cohort study

The Lancet (British edition), 1999-06, Vol.353 (9170), p.2116-2119

1999

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Management of recurrent miscarriage: evaluating the impact of a guideline

Human reproduction (Oxford), 2007-05, Vol.22 (5), p.1298-1303

2007

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A comparison of counselee and counselor satisfaction in reproductive genetic counseling

Clinical genetics, 2007-08, Vol.72 (2), p.74-82

2007

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Reproductive outcome after PGD in couples with recurrent miscarriage carrying a structural chromosome abnormality: a systematic review

Human reproduction update, 2011-07, Vol.17 (4), p.467-475

2011

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Genetic knowledge and counselling skills of Dutch cardiologists: sufficient for the genomics era?

European heart journal, 2003-03, Vol.24 (6), p.560-566

2003

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Heterogeneous nuclear ribonucleoprotein G‐T (HNRNP G‐T) mutations in men with impaired spermatogenesis

Molecular human reproduction, 2004-04, Vol.10 (4), p.265-269

2004

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Inherited unbalanced structural chromosome abnormalities at prenatal chromosome analysis are rarely ascertained through recurrent miscarriage

Prenatal diagnosis, 2008-05, Vol.28 (5), p.408-411

2008

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Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy

Neuromuscular disorders : NMD, 1999-07, Vol.9 (5), p.347-351

1999

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Genetic counseling for familial conditions during pregnancy: an analysis of patient characteristics

Clinical genetics, 2004-08, Vol.66 (2), p.112-121

2004

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Early pregnancy screening for fetal aneuploidy with serum markers and nuchal translucency

Prenatal diagnosis, 1999-05, Vol.19 (5), p.458-462

1999

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Human Synaptonemal Complex Protein 1 (SCP1): Isolation and Characterization of the cDNA and Chromosomal Localization of the Gene

Genomics (San Diego, Calif.), 1997-02, Vol.39 (3), p.377-384

1997

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Development of guideline-based quality indicators for recurrent miscarriage

Reproductive biomedicine online, 2010-02, Vol.20 (2), p.267-273

2010

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Genetic counseling for hereditary cancer: A pilot study on experiences of patients and family members

Patient education and counseling, 1997-09, Vol.32 (1), p.107-116

1997

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Knowledge and perceived risks in couples undergoing genetic testing after recurrent miscarriage or for poor semen quality

Reproductive biomedicine online, 2011-10, Vol.23 (4), p.525-533

2011

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High-resolution localization of 69 potential human zinc finger protein genes: A number are clustered

Genomics (San Diego, Calif.), 1992-02, Vol.12 (2), p.254-263

1992

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Cytogenetic characteristics of ectopic pregnancy

Human reproduction (Oxford), 1996-12, Vol.11 (12), p.2769-2771

1996

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Enlarged nuchal translucency and low serum protein concentrations as possible markers for Zellweger syndrome

Ultrasound in obstetrics & gynecology, 1999-04, Vol.13 (4), p.268-270

1999

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Enrichment, identification and analysis of fetal cells from maternal blood: evaluation of a prenatal diagnosis system

Prenatal diagnosis, 1999-07, Vol.19 (7), p.648-652

1999

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Qigong: a personal experience

Alternative therapies in health and medicine, 2000-09, Vol.6 (5), p.98

Leschot, N J

2000

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Co-variables in first trimester maternal serum screening

Prenatal diagnosis, 2000-03, Vol.20 (3), p.186-189

2000

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Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy

Consecutive or non-consecutive recurrent miscarriage: is there any difference in carrier status?

Clinical relevance of diagnosing structural chromosome abnormalities in couples with repeated miscarriage

Mutations in the testis-specific NALP14 gene in men suffering from spermatogenic failure

Genetic aspects of miscarriage

Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in the Netherlands: a cohort study

Management of recurrent miscarriage: evaluating the impact of a guideline

A comparison of counselee and counselor satisfaction in reproductive genetic counseling

Reproductive outcome after PGD in couples with recurrent miscarriage carrying a structural chromosome abnormality: a systematic review

Genetic knowledge and counselling skills of Dutch cardiologists: sufficient for the genomics era?

Heterogeneous nuclear ribonucleoprotein G‐T (HNRNP G‐T) mutations in men with impaired spermatogenesis

Inherited unbalanced structural chromosome abnormalities at prenatal chromosome analysis are rarely ascertained through recurrent miscarriage

Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy

Genetic counseling for familial conditions during pregnancy: an analysis of patient characteristics

Early pregnancy screening for fetal aneuploidy with serum markers and nuchal translucency

Human Synaptonemal Complex Protein 1 (SCP1): Isolation and Characterization of the cDNA and Chromosomal Localization of the Gene

Development of guideline-based quality indicators for recurrent miscarriage

Genetic counseling for hereditary cancer: A pilot study on experiences of patients and family members

Knowledge and perceived risks in couples undergoing genetic testing after recurrent miscarriage or for poor semen quality

High-resolution localization of 69 potential human zinc finger protein genes: A number are clustered

Cytogenetic characteristics of ectopic pregnancy

Enlarged nuchal translucency and low serum protein concentrations as possible markers for Zellweger syndrome

Enrichment, identification and analysis of fetal cells from maternal blood: evaluation of a prenatal diagnosis system

Qigong: a personal experience

Co-variables in first trimester maternal serum screening

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