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EPCAM germline and somatic rearrangements in lynch syndrome: identification of a novel 3′EPCAM deletion

Genes chromosomes & cancer, 2013-09, Vol.52 (9), p.845-854

2013

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Intratumoral heterogeneity in colorectal cancer: Can histology be used as a guidance for molecular testing?

Journal of clinical oncology, 2017-02, Vol.35 (4_suppl), p.611-611

2017

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Phosphatidylinositol‐4,5‐bisphosphate 3‐kinase catalytic subunit alpha (PIK3CA)‐related overgrowth spectrum: A brief report

Pediatric dermatology, 2018-05, Vol.35 (3), p.e186-e188

2018

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Keratinocytic epidermal nevus syndrome with Schwann cell proliferation, lipomatous tumour and mosaic KRAS mutation

BMC medical genetics, 2015-02, Vol.16 (1), p.6-6, Article 6

2015

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Primary role of the HLA class II DRB10301 allele in graves disease

American journal of medical genetics, 2000-12, Vol.95 (5), p.432-437

2000

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EPCAM germline and somatic rearrangements in Lynch syndrome: identification of a novel 3'EPCAM deletion

Genes chromosomes & cancer, 2013-09, Vol.52 (9), p.845-854

2013

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Recurrent Multilocular Mandibular Giant Cell Granuloma in Neurofibromatosis Type 1: Evidence for Second Hit Mutation of NF1 Gene in the Jaw Lesion and Treatment with Curettage and Bone Substitute Materials

Journal of cranio-maxillo-facial surgery, 2016-08, Vol.44 (8), p.1054-1060

2016

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The clinical relevance of microsatellite alterations in head and neck squamous cell carcinoma: a critical review

European journal of human genetics : EJHG, 2007-07, Vol.15 (7), p.734-741

2007

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Analysis of microsatellite instability in gastric mucosa-associated lymphoid tissue lymphoma

Leukemia & lymphoma, 2013-04, Vol.54 (4), p.812-818

2013

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prevalence of microsatellite instability in head and neck squamous cell carcinoma

Journal of cancer research and clinical oncology, 2009-03, Vol.135 (3), p.485-490

2009

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Detection of bacterial and mycoplasma contamination in cell cultures by polymerase chain reaction

FEMS microbiology letters, 1992-11, Vol.99 (1), p.89-94

1992

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Increased prevalence of migraine in adult congenital heart disease

Heart (British Cardiac Society), 2007-03, Vol.93 (3), p.361-362

2007

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Microsatellite alterations in head and neck squamous cell carcinoma and relation to expression of pimonidazole, CA IX and GLUT-1

Radiotherapy and oncology, 2006-08, Vol.80 (2), p.143-150

2006

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Mutation analysis in Belgian familial colorectal cancer kindreds: High proportion of novel mutations in the mismatch repair genes

Gastroenterology (New York, N.Y. 1943), 2000-04, Vol.118 (4), p.A1413-A1413

2000

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Increased and decreased relative risk for noninsulin-dependent diabetes mellitus conferred by HLA class II and by CD4 alleles

Clinical genetics, 1995-05, Vol.47 (5), p.225-230

1995

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Post-translational modification of the β-subunit of the human fibronectin receptor

FEBS letters, 1988-04, Vol.231 (2), p.402-406

1988

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Study of the possible association of HLA class II, CD4, and CD3 polymorphisms with schizophrenia

American journal of medical genetics, 1994-12, Vol.54 (4), p.372-377

1994

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Mapping of human fibronectin receptor? subunit gene to chromosome 10

Somatic cell and molecular genetics, 1988-01, Vol.14 (1), p.99-104

1988

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Mapping of human fibronectin receptor β subunit gene to chromosome 10

Somatic cell and molecular genetics, 1988, Vol.14 (1), p.99-104

1988

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Monoclonal antibody DH12 reacts with a cell surface and a precursor form of the β subunit of the human fibronectin receptor

Cell biology international reports, 1988, Vol.12 (1), p.9-16

1988

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EPCAM germline and somatic rearrangements in lynch syndrome: identification of a novel 3′EPCAM deletion

Intratumoral heterogeneity in colorectal cancer: Can histology be used as a guidance for molecular testing?

Phosphatidylinositol‐4,5‐bisphosphate 3‐kinase catalytic subunit alpha (PIK3CA)‐related overgrowth spectrum: A brief report

Keratinocytic epidermal nevus syndrome with Schwann cell proliferation, lipomatous tumour and mosaic KRAS mutation

Primary role of the HLA class II DRB10301 allele in graves disease

EPCAM germline and somatic rearrangements in Lynch syndrome: identification of a novel 3'EPCAM deletion

Recurrent Multilocular Mandibular Giant Cell Granuloma in Neurofibromatosis Type 1: Evidence for Second Hit Mutation of NF1 Gene in the Jaw Lesion and Treatment with Curettage and Bone Substitute Materials

The clinical relevance of microsatellite alterations in head and neck squamous cell carcinoma: a critical review

Analysis of microsatellite instability in gastric mucosa-associated lymphoid tissue lymphoma

prevalence of microsatellite instability in head and neck squamous cell carcinoma

Detection of bacterial and mycoplasma contamination in cell cultures by polymerase chain reaction

Increased prevalence of migraine in adult congenital heart disease

Microsatellite alterations in head and neck squamous cell carcinoma and relation to expression of pimonidazole, CA IX and GLUT-1

Mutation analysis in Belgian familial colorectal cancer kindreds: High proportion of novel mutations in the mismatch repair genes

Increased and decreased relative risk for noninsulin-dependent diabetes mellitus conferred by HLA class II and by CD4 alleles

Post-translational modification of the β-subunit of the human fibronectin receptor

Study of the possible association of HLA class II, CD4, and CD3 polymorphisms with schizophrenia

Mapping of human fibronectin receptor? subunit gene to chromosome 10

Mapping of human fibronectin receptor β subunit gene to chromosome 10

Monoclonal antibody DH12 reacts with a cell surface and a precursor form of the β subunit of the human fibronectin receptor

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