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Genetic risk factors in infertile men with severe oligozoospermia and azoospermia

Human reproduction (Oxford), 2002-01, Vol.17 (1), p.13-16

2002

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Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience

European journal of human genetics : EJHG, 1998-06, Vol.6 (3), p.194-200

1998

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Determination of the parent of origin in nine cases of prenatally detected chromosome aberrations found after intracytoplasmic sperm injection

Human reproduction (Oxford), 1997-04, Vol.12 (4), p.682-686

1997

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Interchromosomal insertions: Identification of five cases and a review

Human genetics, 2000-11, Vol.107 (5), p.415-432

2000

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ETIOLOGICAL STUDIES OF SEVERE OR FAMILIAL HYPOSPADIAS

The Journal of urology, 2001-04, Vol.165 (4), p.1246-1254

2001

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Genetic counselling before intracytoplasmic sperm injection

The Lancet (British edition), 1997-08, Vol.350 (9076), p.490-490

1997

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Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype

Journal of medical genetics, 1993-09, Vol.30 (9), p.761-766

1993

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An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito

Journal of medical genetics, 2000-04, Vol.37 (4), p.287-291

2000

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Chromosome 22q11 deletions in patients with selected outflow tract malformations

Genetic counseling, 1999, Vol.10 (1), p.35

1999

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Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmic sperm injection

Human reproduction (Oxford), 1997-08, Vol.12 (8), p.1642-1644

1997

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Molecular detection of a translocation (Y;11)(q11.2;q24) in a 45,X male with signs of Jacobsen syndrome

Human genetics, 1992-03, Vol.88 (6), p.661-667

1992

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Molecular Cytogenetic Analysis of Eight Inversion Duplications of Human Chromosome 13q That Each Contain a Neocentromere

American journal of human genetics, 2000-06, Vol.66 (6), p.1794-1806

2000

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Application of fluorescent in situ hybridization for 'de novo' anomalies in prenatal diagnosis

Prenatal diagnosis, 1993-09, Vol.13 (9), p.825-832

1993

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Recurrence of DiGeorge syndrome: prenatal detection by FISH of a molecular 22q11 deletion

Journal of medical genetics, 1995-08, Vol.32 (8), p.657-658

1995

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Avoidance of emergency surgery in newborn infants with trisomy 18

The Lancet (British edition), 1992-04, Vol.339 (8798), p.913-915

1992

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Comparing mortality and morbidity in hospitals: theory and practice of quality assessment in peer review

Methods of information in medicine, 1994-05, Vol.33 (2), p.196-204

1994

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Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome

Journal of medical genetics, 1992-12, Vol.29 (12), p.853-857

1992

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Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family

Journal of medical genetics, 1996-12, Vol.33 (12), p.1007-1010

1996

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Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience

European journal of human genetics : EJHG, 1998-05, Vol.6 (3), p.194-200

1998

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DNA diagnosis of Prader-Willi and Angelman syndromes with the probe PW71 (D15S63)

Human genetics, 1995-05, Vol.95 (5), p.562-567

1995

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The Perinatal Database of the Netherlands

European journal of obstetrics & gynecology and reproductive biology, 2001, Vol.94 (1), p.125-138

2001

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A chromosome 21-specific cosmid cocktail for the detection of chromosome 21 aberrations in interphase nuclei

Prenatal diagnosis, 1995-08, Vol.15 (8), p.705-711

1995

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Randomised clinical trial on the effect of the Dutch obstetric peer review system

European journal of obstetrics & gynecology and reproductive biology, 2002-04, Vol.102 (1), p.21-30

2002

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Prenatal cytogenetic and postnatal molecular studies on 46,XX male

The Lancet (British edition), 1992-01, Vol.339 (8786), p.180-181

1992

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First trimester diagnosis from chorionic villi of a der(15),t(9;15)(q33;q14)mat identified by DA/DAPI staining

Journal of medical genetics, 1986-02, Vol.23 (1), p.89-90

1986

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Genetic risk factors in infertile men with severe oligozoospermia and azoospermia

Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience

Determination of the parent of origin in nine cases of prenatally detected chromosome aberrations found after intracytoplasmic sperm injection

Interchromosomal insertions: Identification of five cases and a review

ETIOLOGICAL STUDIES OF SEVERE OR FAMILIAL HYPOSPADIAS

Genetic counselling before intracytoplasmic sperm injection

Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype

An unbalanced submicroscopic translocation t(8;16)(q24.3;p13.3)pat associated with tuberous sclerosis complex, adult polycystic kidney disease, and hypomelanosis of Ito

Chromosome 22q11 deletions in patients with selected outflow tract malformations

Two cases of Robertsonian translocations in oligozoospermic males and their consequences for pregnancies induced by intracytoplasmic sperm injection

Molecular detection of a translocation (Y;11)(q11.2;q24) in a 45,X male with signs of Jacobsen syndrome

Molecular Cytogenetic Analysis of Eight Inversion Duplications of Human Chromosome 13q That Each Contain a Neocentromere

Application of fluorescent in situ hybridization for 'de novo' anomalies in prenatal diagnosis

Recurrence of DiGeorge syndrome: prenatal detection by FISH of a molecular 22q11 deletion

Avoidance of emergency surgery in newborn infants with trisomy 18

Comparing mortality and morbidity in hospitals: theory and practice of quality assessment in peer review

Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome

Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family

Chromosome studies in 1792 males prior to intra-cytoplasmic sperm injection: the Dutch experience

DNA diagnosis of Prader-Willi and Angelman syndromes with the probe PW71 (D15S63)

The Perinatal Database of the Netherlands

A chromosome 21-specific cosmid cocktail for the detection of chromosome 21 aberrations in interphase nuclei

Randomised clinical trial on the effect of the Dutch obstetric peer review system

Prenatal cytogenetic and postnatal molecular studies on 46,XX male

First trimester diagnosis from chorionic villi of a der(15),t(9;15)(q33;q14)mat identified by DA/DAPI staining

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