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Tumor risk in Beckwith-Wiedemann syndrome: A review and meta-analysis

American journal of medical genetics. Part A, 2005-07, Vol.136A (1), p.95-104

2005

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T.P.2

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.860-861

2014

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Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals

European journal of medical genetics, 2009-03, Vol.52 (2), p.77-87

2009

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Circulating matrix γ‐carboxyglutamate protein (MGP) species are refractory to vitamin K treatment in a new case of Keutel syndrome

Journal of thrombosis and haemostasis, 2011-06, Vol.9 (6), p.1225-1235

2011

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T.P.2: The age of ambulation in boys with Duchenne muscular dystrophy and its use as an end-point in clinical trials

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9-10), p.860-861

2014

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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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Forty-Five Years of Duchenne Muscular Dystrophy in The Netherlands

Journal of neuromuscular diseases, 2014, Vol.1 (1), p.99-109

2014

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Wilms tumour as a possible early manifestation of hereditary leiomyomatosis and renal cell cancer?

British journal of dermatology (1951), 2009-03, Vol.160 (3), p.707-709

2009

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Response to Fukuzawa et al. correspondence "Correct Usage of Loss Imprinting"

American journal of medical genetics. Part A, 2005-11, Vol.138A (4), p.413-414

2005

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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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Neurofibromatosis type I and pregnancy: a fatal attraction?: Development of malignant schwannoma during pregnancy in a patient with neurofibromatosis type I

BJOG : an international journal of obstetrics and gynaecology, 2003-05, Vol.110 (5), p.530-532

2003

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Severe complications in a child with achondroplasia and two FGFR3 mutations on the same allele

American journal of medical genetics. Part A, 2006-02, Vol.140A (3), p.284-290

2006

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Malpuech syndrome: Three patients and a review

American journal of medical genetics. Part A, 2005-05, Vol.134A (4), p.450-453

2005

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Neurofibromatosis type I and pregnancy: a fatal attraction?

BJOG : an international journal of obstetrics and gynaecology, 2003-05, Vol.110 (5), p.530-532

2003

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Neurofibromatosis type I and pregnancy: a fatal attraction?: Development of malignant schwannoma during pregnancy in a patient with neurofibromatosis type I

BJOG : an international journal of obstetrics and gynaecology, 2003-05, Vol.110 (5), p.530-532

2003

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A novel γ-sarcoglycan mutation causing childhood onset, slowly progressive limb girdle muscular dystrophy

Neuromuscular disorders : NMD, 1998-06, Vol.8 (5), p.305-308

1998

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Long-range genomic map of the Duchenne muscular dystrophy (DMD) gene: Isolation and use of J66 (DXS268), a distal intragenic marker

Genomics (San Diego, Calif.), 1987-12, Vol.1 (4), p.329-336

1987

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Two cases of the caudal duplication anomaly including a discordant monozygotic twin

American journal of medical genetics, 2002-11, Vol.112 (4), p.390-393

2002

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T. van Els, G. Extra, Ch. van Os, Th. Bongaerts, "Handboek voor de Toegepaste Taalkunde, het leren en onderwijzen van moderne vreemde talen" (Book Review)

Forum der Letteren, 1979, Vol.20 (1), p.61

Essen, A.J. van

1979

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Over de Ontwikkeling, Vernieuwing en Verduidelijking van Doelstellingen Voor het Vreemde-Taalonderwijs

Toegepaste Taalwetenschap in Artikelen, 1982-01, Vol.14, p.22-44

1982

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Malpuech syndrome: Three patients and a review

American Journal of Medical Genetics Part A, 2005, Vol.134A (4), p.450-453

2005

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Severe complications in a child with achondroplasia and two FGFR3 mutations on the same allele

American Journal of Medical Genetics Part A, 2006, Vol.140A (3), p.284-290

2006

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Two cases of the caudal duplication anomaly including a discordant monozygotic twin

American Journal of Medical Genetics, 2002, Vol.112 (4), p.390-393

2002

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Kognmeve Stijl en Onderwijsdifferentiatie

Toegepaste Taalwetenschap in Artikelen, 1990-01, Vol.37, p.35-44

1990

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Over Het Meten Van Grammatikale Kennis Van Het Engels En Verband Tussen De Testprestaties Van Leerlingen En De Aard Van Grammatikale Regels En Subsystemen

Toegepaste Taalwetenschap in Artikelen, 1985-01, Vol.23, p.90-111

1985

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Tumor risk in Beckwith-Wiedemann syndrome: A review and meta-analysis

T.P.2

Extending the phenotype of recurrent rearrangements of 16p11.2: Deletions in mentally retarded patients without autism and in normal individuals

Circulating matrix γ‐carboxyglutamate protein (MGP) species are refractory to vitamin K treatment in a new case of Keutel syndrome

T.P.2: The age of ambulation in boys with Duchenne muscular dystrophy and its use as an end-point in clinical trials

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

Forty-Five Years of Duchenne Muscular Dystrophy in The Netherlands

Wilms tumour as a possible early manifestation of hereditary leiomyomatosis and renal cell cancer?

Response to Fukuzawa et al. correspondence "Correct Usage of Loss Imprinting"

Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy

Neurofibromatosis type I and pregnancy: a fatal attraction?: Development of malignant schwannoma during pregnancy in a patient with neurofibromatosis type I

Severe complications in a child with achondroplasia and two FGFR3 mutations on the same allele

Malpuech syndrome: Three patients and a review

Neurofibromatosis type I and pregnancy: a fatal attraction?

Neurofibromatosis type I and pregnancy: a fatal attraction?: Development of malignant schwannoma during pregnancy in a patient with neurofibromatosis type I

A novel γ-sarcoglycan mutation causing childhood onset, slowly progressive limb girdle muscular dystrophy

Long-range genomic map of the Duchenne muscular dystrophy (DMD) gene: Isolation and use of J66 (DXS268), a distal intragenic marker

Two cases of the caudal duplication anomaly including a discordant monozygotic twin

T. van Els, G. Extra, Ch. van Os, Th. Bongaerts, "Handboek voor de Toegepaste Taalkunde, het leren en onderwijzen van moderne vreemde talen" (Book Review)

Over de Ontwikkeling, Vernieuwing en Verduidelijking van Doelstellingen Voor het Vreemde-Taalonderwijs

Malpuech syndrome: Three patients and a review

Severe complications in a child with achondroplasia and two FGFR3 mutations on the same allele

Two cases of the caudal duplication anomaly including a discordant monozygotic twin

Kognmeve Stijl en Onderwijsdifferentiatie

Over Het Meten Van Grammatikale Kennis Van Het Engels En Verband Tussen De Testprestaties Van Leerlingen En De Aard Van Grammatikale Regels En Subsystemen

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