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Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands

Netherlands heart journal, 2010-05, Vol.18 (5), p.248-254

2010

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Pearson syndrome and the role of deletion dimers and duplications in the mtDNA

Journal of inherited metabolic disease, 2004-01, Vol.27 (1), p.47-55

2004

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A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome

Human molecular genetics, 1994-04, Vol.3 (4), p.615-620

1994

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Molecular genetics of inherited long Qt syndromes

European heart journal, 1998-10, Vol.19 (10), p.1427-1433

1998

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Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands

Netherlands heart journal, 2010-05, Vol.18 (5), p.248-254

2010

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Human lens γ-crystallin sequences are located in the p12-qter region of chromosome 2

Human genetics, 1985-01, Vol.70 (3), p.217-221

1985

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The long QT syndrome : a novel missense mutation in the S6 region of the KVLQT1 gene

Human genetics, 1997-09, Vol.100 (3-4), p.356-361

1997

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On the origin of recurrent trisomy 21: determination using chromosomal and DNA polymorphisms

Clinical genetics, 1987-12, Vol.32 (6), p.409-413

1987

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Methods in molecular cardiology: DHPLC mutation detection analysis

Netherlands heart journal, 2005-01, Vol.13 (1), p.11-17

2005

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Human gametes and zygotes studied by nonradioactive in situ hybridization

Cytogenetic and genome research, 1990, Vol.53 (1), p.15-19

1990

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Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping

Human genetics, 1989-10, Vol.83 (3), p.280-286

1989

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Characterization of the rat γ-crystallin gene family and its expression in the eye lens

Journal of molecular biology, 1985-04, Vol.182 (3), p.419-430

1985

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RFLP haplotyping and mutation analysis of the phenylalamine hydroxylase gene in Dutch phenylketonuria families

Human genetics, 1993, Vol.92 (6), p.588-592

1993

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Human adult cardiac autonomic innervation: Controversies in anatomical knowledge and relevance for cardiac neuromodulation

Autonomic neuroscience, 2020-09, Vol.227, p.102674-102674, Article 102674

2020

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Rate of recombination of chromosomes 21 in parents of children with Down syndrome

Clinical genetics, 1990-06, Vol.37 (6), p.463-469

1990

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Noninvasive visualization of the cardiac venous system using multislice computed tomography

Journal of the American College of Cardiology, 2005-03, Vol.45 (5), p.749-753

2005

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Sacubitril/valsartan in the treatment of systemic right ventricular failure

Heart (British Cardiac Society), 2021-01, Vol.107 (21), p.1725-1730

2021

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Pulmonary ductal coarctation and left pulmonary artery interruption; pathology and role of neural crest and second heart field during development

PloS one, 2020-05, Vol.15 (5), p.e0228478-e0228478

2020

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Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy

European heart journal, 2014-08, Vol.35 (32), p.2165-2173

2014

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The association between pro-inflammatory biomarkers and nonspecific low back pain: a systematic review

The spine journal, 2018-11, Vol.18 (11), p.2140-2151

2018

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Long-term outcome after atrial correction for transposition of the great arteries

Heart (British Cardiac Society), 2019-05, Vol.105 (10), p.790-796

2019

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A new prediction model for ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy

European heart journal, 2019-06, Vol.40 (23), p.1850-1858

2019

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Asymmetry and Heterogeneity: Part and Parcel in Cardiac Autonomic Innervation and Function

Frontiers in physiology, 2021-09, Vol.12, p.665298

2021

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Coding of coronary arterial origin and branching in congenital heart disease: The modified Leiden Convention

The Journal of thoracic and cardiovascular surgery, 2018-12, Vol.156 (6), p.2260-2269

2018

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Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands

Pearson syndrome and the role of deletion dimers and duplications in the mtDNA

A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome

Molecular genetics of inherited long Qt syndromes

Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands

Human lens γ-crystallin sequences are located in the p12-qter region of chromosome 2

The long QT syndrome : a novel missense mutation in the S6 region of the KVLQT1 gene

On the origin of recurrent trisomy 21: determination using chromosomal and DNA polymorphisms

Methods in molecular cardiology: DHPLC mutation detection analysis

Human gametes and zygotes studied by nonradioactive in situ hybridization

Distribution of meiotic recombination along nondisjunction chromosomes 21 in Down syndrome determined using cytogenetics and RFLP haplotyping

Characterization of the rat γ-crystallin gene family and its expression in the eye lens

RFLP haplotyping and mutation analysis of the phenylalamine hydroxylase gene in Dutch phenylketonuria families

MUSCLEMOTION: A Versatile Open Software Tool to Quantify Cardiomyocyte and Cardiac Muscle Contraction In Vitro and In Vivo

Human adult cardiac autonomic innervation: Controversies in anatomical knowledge and relevance for cardiac neuromodulation

Rate of recombination of chromosomes 21 in parents of children with Down syndrome

Noninvasive visualization of the cardiac venous system using multislice computed tomography

Sacubitril/valsartan in the treatment of systemic right ventricular failure

Pulmonary ductal coarctation and left pulmonary artery interruption; pathology and role of neural crest and second heart field during development

Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy

The association between pro-inflammatory biomarkers and nonspecific low back pain: a systematic review

Long-term outcome after atrial correction for transposition of the great arteries

A new prediction model for ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy

Asymmetry and Heterogeneity: Part and Parcel in Cardiac Autonomic Innervation and Function

Coding of coronary arterial origin and branching in congenital heart disease: The modified Leiden Convention

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