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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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Reproductive outcome after chromosome analysis in couples with two or more miscarriages: case-control study

BMJ, 2006-04, Vol.332 (7544), p.759-763

International edition, 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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Selective chromosome analysis in couples with two or more miscarriages: case-control study

BMJ, 2005-07, Vol.331 (7509), p.137-141

International edition, 2005

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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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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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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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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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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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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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Reduced copy number of DAZ genes in subfertile and infertile men

Fertility and sterility, 2002, Vol.77 (1), p.68-75

2002

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Familial clustering of impaired spermatogenesis: no evidence for a common genetic inheritance pattern

Human reproduction (Oxford), 2004-01, Vol.19 (1), p.71-76

2004

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Counselor–counselee interaction in reproductive genetic counseling: Does a pregnancy in the counselee make a difference?

Patient education and counseling, 2006, Vol.60 (1), p.80-90

2006

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Mutations in the human BOULE gene are not a major cause of impaired spermatogenesis

Fertility and sterility, 2005-02, Vol.83 (2), p.513-515

2005

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Referral for genetic counselling during pregnancy: limited alertness and awareness about genetic risk factors among GPs

Family practice, 2003-04, Vol.20 (2), p.135-141

2003

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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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Clinical relevance of partial AZFc deletions

Fertility and sterility, 2002-12, Vol.78 (6), p.1209-1214

2002

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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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Chromosomal region 11p15 is associated with male factor subfertility

Molecular human reproduction, 2003-10, Vol.9 (10), p.587-592

2003

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Absence of deleted in azoospermia ( DAZ) genes in spermatozoa of infertile men with somatic DAZ deletions

Fertility and sterility, 2001-03, Vol.75 (3), p.476-479

2001

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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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Partial DAZ deletions in a family with five infertile brothers

Fertility and sterility, 2003-06, Vol.79, p.1652-1655

2003

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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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The use of spermHALO‐FISH to determine DAZ gene copy number

Molecular human reproduction, 2003-04, Vol.9 (4), p.183-188

2003

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A placental diploid cell line is not essential for ongoing trisomy 13 or 18 pregnancies

European journal of human genetics : EJHG, 2001-04, Vol.9 (4), p.286-290

2001

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

Reproductive outcome after chromosome analysis in couples with two or more miscarriages: case-control study

Genetic aspects of miscarriage

Selective chromosome analysis in couples with two or more miscarriages: case-control study

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

A comparison of counselee and counselor satisfaction in reproductive genetic counseling

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

Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy

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

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

Reduced copy number of DAZ genes in subfertile and infertile men

Familial clustering of impaired spermatogenesis: no evidence for a common genetic inheritance pattern

Counselor–counselee interaction in reproductive genetic counseling: Does a pregnancy in the counselee make a difference?

Mutations in the human BOULE gene are not a major cause of impaired spermatogenesis

Referral for genetic counselling during pregnancy: limited alertness and awareness about genetic risk factors among GPs

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

Clinical relevance of partial AZFc deletions

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

Chromosomal region 11p15 is associated with male factor subfertility

Absence of deleted in azoospermia ( DAZ) genes in spermatozoa of infertile men with somatic DAZ deletions

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

Partial DAZ deletions in a family with five infertile brothers

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

The use of spermHALO‐FISH to determine DAZ gene copy number

A placental diploid cell line is not essential for ongoing trisomy 13 or 18 pregnancies

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