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A newly recognised microdeletion syndrome involving 2p15p16.1: narrowing down the critical region by adding another patient detected by genome wide tiling path array comparative genomic hybridisation analysis

Journal of medical genetics, 2008-02, Vol.45 (2), p.122-124

2008

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Cryptic duplication of the distal segment of 22q due to a translocation (21;22): three case reports and a review of the literature

European journal of medical genetics, 2006-09, Vol.49 (5), p.384-395

2006

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A new case of dup(1)(q21.2q12) in an individual with mild mental retardation

Genetic counseling, 2003, Vol.14 (4), p.407

2003

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Down-Turner syndrome: case report and review

Journal of medical genetics, 1994-10, Vol.31 (10), p.807-810

1994

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Identification of an unbalanced cryptic translocation between the chromosomes 8 and 13 in two sisters with mild mental retardation accompanied by mild dysmorphic features

European journal of human genetics : EJHG, 2000-08, Vol.8 (8), p.637-640

2000

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Dysmorphology and mental retardation: molecular cytogenetic studies in dysmorphic mentally retarded patients

Annales de génétique, 2001-04, Vol.44 (2), p.89-92

2001

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A newly recognised microdeletion syndrome involving 2p15p16.1: narrowing down the critical region by adding another patient detected by genome wide tiling path array comparative genomic hybridisation analysis

Journal of medical genetics, 2008, Vol.45 (2), p.122-124

2008

Volltextzugriff (PDF)

The Strengths and Difficulties Questionnaire Parent Form: Dutch norms and validity

BMC pediatrics, 2022-04, Vol.22 (1), p.202-202, Article 202

2022

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Validation of the SDQ in a multi-ethnic population of young children

European journal of public health, 2014-02, Vol.24 (1), p.26-32

2014

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Ethnic differences in problem perception and perceived need for care for young children with problem behaviour

Journal of child psychology and psychiatry, 2012-10, Vol.53 (10), p.1063-1071

2012

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Ethnicity, socioeconomic position and severity of problems as predictors of mental health care use in 5- to 8-year-old children with problem behaviour

Social Psychiatry and Psychiatric Epidemiology, 2014-05, Vol.49 (5), p.733-742

2014

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Ethnic differences in problem perception and perceived need as determinants of referral in young children with problem behaviour

European child & adolescent psychiatry, 2014-05, Vol.23 (5), p.273-281

2014

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Seasonal variation in self-reported health and health-related behaviour in Dutch adolescents

Public health (London), 2009-10, Vol.123 (10), p.686-688

2009

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Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations: Noninvasive prenatal testing by two-channel SBS

Prenatal diagnosis, 2016-03, Vol.36 (3), p.216-223

2016

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Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations

Prenatal diagnosis, 2016-03, Vol.36 (3), p.216-223

2016

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Buccal cell FISH and blood PCR-Y detect high rates of X chromosomal mosaicism and Y chromosomal derivatives in patients with Turner syndrome

European journal of medical genetics, 2013-09, Vol.56 (9), p.497-501

2013

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Further refinement of the candidate region for monosomy 9p syndrome

American journal of medical genetics. Part A, 2007-10, Vol.143A (19), p.2353-2356

2007

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Further refinement of the candidate region for monosomy 9p syndrome

American journal of medical genetics. Part A, 2007, Vol.143A (19), p.2353-2356

2007

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A newly recognised microdeletion syndrome involving 2p15p16.1: narrowing down the critical region by adding another patient detected by genome wide tiling path array comparative genomic hybridisation analysis

Cryptic duplication of the distal segment of 22q due to a translocation (21;22): three case reports and a review of the literature

A new case of dup(1)(q21.2q12) in an individual with mild mental retardation

Down-Turner syndrome: case report and review

Identification of an unbalanced cryptic translocation between the chromosomes 8 and 13 in two sisters with mild mental retardation accompanied by mild dysmorphic features

Dysmorphology and mental retardation: molecular cytogenetic studies in dysmorphic mentally retarded patients

A newly recognised microdeletion syndrome involving 2p15p16.1: narrowing down the critical region by adding another patient detected by genome wide tiling path array comparative genomic hybridisation analysis

The Strengths and Difficulties Questionnaire Parent Form: Dutch norms and validity

Validation of the SDQ in a multi-ethnic population of young children

Ethnic differences in problem perception and perceived need for care for young children with problem behaviour

Ethnicity, socioeconomic position and severity of problems as predictors of mental health care use in 5- to 8-year-old children with problem behaviour

Ethnic differences in problem perception and perceived need as determinants of referral in young children with problem behaviour

Seasonal variation in self-reported health and health-related behaviour in Dutch adolescents

Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations: Noninvasive prenatal testing by two-channel SBS

Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations

Buccal cell FISH and blood PCR-Y detect high rates of X chromosomal mosaicism and Y chromosomal derivatives in patients with Turner syndrome

Further refinement of the candidate region for monosomy 9p syndrome

Further refinement of the candidate region for monosomy 9p syndrome

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