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Case report: The child- and adolescent psychiatric phenotype of a brother and sister with 16p11.2 microduplication

Tijdschrift voor psychiatrie, 2016, Vol.58 (4), p.318-322

2016

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From gene to disease; presenilins and Alzheimer disease

Nederlands tijdschrift voor geneeskunde, 2001-10, Vol.145 (42), p.2027

2001

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Genetics and male infertility

Verhandelingen - Koninklijke Academie voor Geneeskunde van Belgie, 2009, Vol.71 (3), p.115

2009

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Immunology in medical practice. XXVI. Immunogenetics of chronic inflammatory bowel diseases

Nederlands tijdschrift voor geneeskunde, 1999-11, Vol.143 (48), p.2414

1999

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Adaptive skills, cognitive functioning and behavioural problems in adolescents with 22q11.2 deletion syndrome

Tijdschrift voor psychiatrie, 2013, Vol.55 (5), p.369-374

2013

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A girl with 16p11.2 deletion syndrome

Nederlands tijdschrift voor geneeskunde, 2019-03, Vol.163

2019

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From gene to disease; hypophosphataemic rickets and the PHEX gene

Nederlands tijdschrift voor geneeskunde, 2006-09, Vol.150 (37), p.2058

2006

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From gene to disease; hypophosphataemic rickets and the PHEX gene

Nederlands tijdschrift voor geneeskunde, 2006-06, Vol.150 (25), p.1390

2006

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The importance of comprehensive transition of care in women with Turner's syndrome

Nederlands tijdschrift voor geneeskunde, 2007-07, Vol.151 (29), p.1612

Keizer-Schrama, S M P F de Muinck

2007

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Sleep disturbances in Smith-Magenis syndrome: treatment with melatonin and beta-adrenergic antagonists

Tijdschrift voor psychiatrie, 2010, Vol.52 (10), p.719-723

2010

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Mild mental retardation and complex psychiatric symptoms are accompanied by submicroscopic sub-telomeric deletion of a long arm of chromosome 3. A case study

Tijdschrift voor psychiatrie, 2007, Vol.49 (6), p.405-409

2007

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Basal cell naevus syndrome as the cause of a chronic foot ulcer

Nederlands tijdschrift voor geneeskunde, 2006-09, Vol.150 (37), p.2043

2006

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Maternal uniparental disomy 14; differential diagnosis with Prader-Willi syndrome

Nederlands tijdschrift voor geneeskunde, 2015, Vol.159, p.A8240

2015

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Expression of the cystic fibrosis gene in the lungs

Nederlands tijdschrift voor geneeskunde, 2004-04, Vol.148 (17), p.816

2004

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From gene to disease: basal cell naevus syndrome

Nederlands tijdschrift voor geneeskunde, 2005-01, Vol.149 (2), p.78

2005

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From gene to disease; amyloid-beta precursor protein gene instrumental in hereditary cerebral amyloid angiopathies

Nederlands tijdschrift voor geneeskunde, 2001-08, Vol.145 (34), p.1639

2001

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From gene to disease; hereditary multiple exostoses

Nederlands tijdschrift voor geneeskunde, 2002-01, Vol.146 (4), p.162

2002

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Cerebrotendinous xanthomatosis

Nederlands tijdschrift voor geneeskunde, 2001-09, Vol.145 (35), p.1673

Verrips, A

2001

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From gene to disease; from CACNA1A to migraine

Nederlands tijdschrift voor geneeskunde, 2001-02, Vol.145 (6), p.266

2001

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From genes to disease: from vasopressin-V2-receptor and aquaporine-2 to nephrogenic diabetes insipidus

Nederlands tijdschrift voor geneeskunde, 2000-12, Vol.144 (50), p.2402

2000

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Scoliosis in children with chromosome 22q11.2 deletion syndrome

Nederlands tijdschrift voor geneeskunde, 2012, Vol.156 (4), p.A4298

2012

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From gene to disease; neurofibromatosis type 1

Nederlands tijdschrift voor geneeskunde, 2001-09, Vol.145 (36), p.1736

2001

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From gene to disease; tumor necrosis factor receptor and a syndrome of familial periodic fever

Nederlands tijdschrift voor geneeskunde, 2001-01, Vol.145 (2), p.77

2001

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Immunology in the medical practice. XXVII. Mannose-binding lectin, an important link for nonspecific or hereditary immune reaction

Nederlands tijdschrift voor geneeskunde, 2000-06, Vol.144 (25), p.1214

van Deuren, M

2000

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From gene to disease; HD gene and Huntington disease

Nederlands tijdschrift voor geneeskunde, 2001-11, Vol.145 (44), p.2120

2001

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Case report: The child- and adolescent psychiatric phenotype of a brother and sister with 16p11.2 microduplication

From gene to disease; presenilins and Alzheimer disease

Genetics and male infertility

Immunology in medical practice. XXVI. Immunogenetics of chronic inflammatory bowel diseases

Adaptive skills, cognitive functioning and behavioural problems in adolescents with 22q11.2 deletion syndrome

A girl with 16p11.2 deletion syndrome

From gene to disease; hypophosphataemic rickets and the PHEX gene

From gene to disease; hypophosphataemic rickets and the PHEX gene

The importance of comprehensive transition of care in women with Turner's syndrome

Sleep disturbances in Smith-Magenis syndrome: treatment with melatonin and beta-adrenergic antagonists

Mild mental retardation and complex psychiatric symptoms are accompanied by submicroscopic sub-telomeric deletion of a long arm of chromosome 3. A case study

Basal cell naevus syndrome as the cause of a chronic foot ulcer

Maternal uniparental disomy 14; differential diagnosis with Prader-Willi syndrome

Expression of the cystic fibrosis gene in the lungs

From gene to disease: basal cell naevus syndrome

From gene to disease; amyloid-beta precursor protein gene instrumental in hereditary cerebral amyloid angiopathies

From gene to disease; hereditary multiple exostoses

Cerebrotendinous xanthomatosis

From gene to disease; from CACNA1A to migraine

From genes to disease: from vasopressin-V2-receptor and aquaporine-2 to nephrogenic diabetes insipidus

Scoliosis in children with chromosome 22q11.2 deletion syndrome

From gene to disease; neurofibromatosis type 1

From gene to disease; tumor necrosis factor receptor and a syndrome of familial periodic fever

Immunology in the medical practice. XXVII. Mannose-binding lectin, an important link for nonspecific or hereditary immune reaction

From gene to disease; HD gene and Huntington disease

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