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Marginal zone B-cell lymphomas of different sites share similar cytogenetic and morphologic features

Blood, 1996, Vol.87 (1), p.299-307

1996

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Marginal zone B-cell lymphomas of different sites share similar cytogenetic and morphologic features [see comments]

Blood, 1996-01, Vol.87 (1), p.299-307

1996

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Data storage and DNA banking for biomedical research: informed consent, confidentiality, quality issues, ownership, return of benefits. A professional perspective

European journal of human genetics : EJHG, 2003-12, Vol.11 (S2), p.S88-S122

2003

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Predominance of beta-catenin mutations and beta-catenin dysregulation in sporadic aggressive fibromatosis (desmoid tumor)

Oncogene, 1999-11, Vol.18 (47), p.6615-6620

1999

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Differential Induction of Human Beta‐Defensin Expression by Periodontal Commensals and Pathogens in Periodontal Pocket Epithelial Cells

Journal of periodontology (1970), 2005-08, Vol.76 (8), p.1293-1303

2005

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Characteristic pattern of chromosomal gains and losses in marginal zone B cell lymphoma detected by comparative genomic hybridization

Leukemia, 1997-05, Vol.11 (5), p.747-758

1997

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Towards quality assurance and harmonization of genetic testing services in the European Union

Nature biotechnology, 2004-10, Vol.22 (10), p.1230-1235

2004

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Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation

The Journal of clinical investigation, 1998-01, Vol.101 (2), p.487-496

1998

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Mutations in PMM2 , a phosphomannomutase gene on chromosome 16p13 in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)

Nature genetics, 1997-05, Vol.16 (1), p.88-92

1997

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Quadriceps and Grip Strength Are Related to Vitamin D Receptor Genotype in Elderly Nonobese Women

Journal of bone and mineral research, 1997-12, Vol.12 (12), p.2082-2088

1997

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Lack of Homozygotes for the Most Frequent Disease Allele in Carbohydrate-Deficient Glycoprotein Syndrome Type 1A

American journal of human genetics, 1998-03, Vol.62 (3), p.542-550

1998

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Genetic testing and quality control in diagnostic laboratories

Nature genetics, 2000-07, Vol.25 (3), p.259-260

2000

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CFTR mutations and polymorphisms in male infertility

International journal of andrology, 2004-10, Vol.27 (5), p.251-256

2004

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Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotype

Journal of medical genetics, 2004-08, Vol.41 (8), p.629-633

2004

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Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats

American journal of human genetics, 1996-07, Vol.59 (1), p.16-22

1996

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The TNFα receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosis

Human genetics, 2006-04, Vol.119 (3), p.331-343

2006

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Association of tumour necrosis factor alpha variants with the CF pulmonary phenotype

Thorax, 2005-04, Vol.60 (4), p.320-325

2005

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Influence of Nicotine and Cotinine on Epithelial Colonization by Periodontopathogens

Journal of periodontology (1970), 2005-08, Vol.76 (8), p.1315-1322

2005

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Upregulation of Wilms' tumor gene 1 (WT1) in desmoid tumors

International journal of cancer, 2005-03, Vol.114 (2), p.202-208

2005

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Linkage and association of HLA class II genes with vitiligo in a Dutch population

British journal of dermatology (1951), 2001-07, Vol.145 (1), p.90-94

2001

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Invasion and MMP expression profile in desmoid tumours

British journal of cancer, 2004-04, Vol.90 (7), p.1443-1449

2004

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Lack of association between estrogen receptor genotypes and bone mineral density, fracture history, or muscle strength in elderly women

Journal of bone and mineral research, 1999-09, Vol.14 (9), p.1576-1582

1999

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Influence of the Vitamin D Receptor Gene Alleles on Bone Mineral Density in Postmenopausal and Osteoporotic Women

Journal of bone and mineral research, 1997-02, Vol.12 (2), p.241-247

1997

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Cell surface heparan sulfate proteoglycans from human vascular endothelial cells. Core protein characterization and antithrombin III binding properties

The Journal of biological chemistry, 1992-10, Vol.267 (28), p.20435-20443

1992

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Marginal zone B-cell lymphomas of different sites share similar cytogenetic and morphologic features

Marginal zone B-cell lymphomas of different sites share similar cytogenetic and morphologic features [see comments]

Data storage and DNA banking for biomedical research: informed consent, confidentiality, quality issues, ownership, return of benefits. A professional perspective

Mutations in the amiloride-sensitive epithelial sodium channel in patients with cystic fibrosis-like disease

Predominance of beta-catenin mutations and beta-catenin dysregulation in sporadic aggressive fibromatosis (desmoid tumor)

Differential Induction of Human Beta‐Defensin Expression by Periodontal Commensals and Pathogens in Periodontal Pocket Epithelial Cells

Characteristic pattern of chromosomal gains and losses in marginal zone B cell lymphoma detected by comparative genomic hybridization

Towards quality assurance and harmonization of genetic testing services in the European Union

Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation

Mutations in PMM2 , a phosphomannomutase gene on chromosome 16p13 in carbohydrate-deficient glycoprotein type I syndrome (Jaeken syndrome)

Quadriceps and Grip Strength Are Related to Vitamin D Receptor Genotype in Elderly Nonobese Women

Lack of Homozygotes for the Most Frequent Disease Allele in Carbohydrate-Deficient Glycoprotein Syndrome Type 1A

Genetic testing and quality control in diagnostic laboratories

CFTR mutations and polymorphisms in male infertility

Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotype

Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats

The TNFα receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosis

Association of tumour necrosis factor alpha variants with the CF pulmonary phenotype

Influence of Nicotine and Cotinine on Epithelial Colonization by Periodontopathogens

Upregulation of Wilms' tumor gene 1 (WT1) in desmoid tumors

Linkage and association of HLA class II genes with vitiligo in a Dutch population

Invasion and MMP expression profile in desmoid tumours

Lack of association between estrogen receptor genotypes and bone mineral density, fracture history, or muscle strength in elderly women

Influence of the Vitamin D Receptor Gene Alleles on Bone Mineral Density in Postmenopausal and Osteoporotic Women

Cell surface heparan sulfate proteoglycans from human vascular endothelial cells. Core protein characterization and antithrombin III binding properties

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