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F H Menko

Showing results (71-80 of 81) with videos related to

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Journal of Medical Genetics|February 22, 2014
Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium "Care for CMMR-D" (C4CMMR-D)H F A Vasen, Z Ghorbanoghli, F Bourdeaut, et al.
Springerplus|September 22, 2016
Risk of spontaneous pneumothorax due to air travel and diving in patients with Birt-Hogg-Dubé syndromeP C Johannesma, I van de Beek, J W T van der Wel, et al.
Clinical Genetics|October 11, 2007
Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidatesW W J de Leng, M Jansen, R Carvalho, et al.
Familial Cancer|February 17, 2016
Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriersZ Ghorbanoghli, M H Nieuwenhuis, J J Houwing-Duistermaat, et al.
Clinical Genetics|May 31, 2008
Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genesF H Menko, C M F Kneepkens, N de Leeuw, et al.
Clinical Genetics|July 13, 2010
Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysisD L Smit, A R Mensenkamp, S Badeloe, et al.
Journal of Medical Genetics|September 6, 2005
Cancer risks in BRCA2 families: estimates for sites other than breast and ovaryC J van Asperen, R M Brohet, E J Meijers-Heijboer, et al.
British Journal of Cancer|April 3, 1999
Characteristics of small breast and/or ovarian cancer families with germline mutations in BRCA1 and BRCA2M J Ligtenberg, F B Hogervorst, H W Willems, et al.
Journal of Medical Genetics|August 3, 2006
STK11 status and intussusception risk in Peutz-Jeghers syndromeN Hearle, V Schumacher, F H Menko, et al.
Journal of Medical Genetics|September 6, 2005
Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP)M Nielsen, P F Franken, T H C M Reinards, et al.
Pageof 9

Showing results (71-80 of 81) with videos related to

Sort By:
Pageof 9
Journal of Medical Genetics|February 22, 2014
Guidelines for surveillance of individuals with constitutional mismatch repair-deficiency proposed by the European Consortium "Care for CMMR-D" (C4CMMR-D)H F A Vasen, Z Ghorbanoghli, F Bourdeaut, et al.
Springerplus|September 22, 2016
Risk of spontaneous pneumothorax due to air travel and diving in patients with Birt-Hogg-Dubé syndromeP C Johannesma, I van de Beek, J W T van der Wel, et al.
Clinical Genetics|October 11, 2007
Genetic defects underlying Peutz-Jeghers syndrome (PJS) and exclusion of the polarity-associated MARK/Par1 gene family as potential PJS candidatesW W J de Leng, M Jansen, R Carvalho, et al.
Familial Cancer|February 17, 2016
Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriersZ Ghorbanoghli, M H Nieuwenhuis, J J Houwing-Duistermaat, et al.
Clinical Genetics|May 31, 2008
Variable phenotypes associated with 10q23 microdeletions involving the PTEN and BMPR1A genesF H Menko, C M F Kneepkens, N de Leeuw, et al.
Clinical Genetics|July 13, 2010
Hereditary leiomyomatosis and renal cell cancer in families referred for fumarate hydratase germline mutation analysisD L Smit, A R Mensenkamp, S Badeloe, et al.
Journal of Medical Genetics|September 6, 2005
Cancer risks in BRCA2 families: estimates for sites other than breast and ovaryC J van Asperen, R M Brohet, E J Meijers-Heijboer, et al.
British Journal of Cancer|April 3, 1999
Characteristics of small breast and/or ovarian cancer families with germline mutations in BRCA1 and BRCA2M J Ligtenberg, F B Hogervorst, H W Willems, et al.
Journal of Medical Genetics|August 3, 2006
STK11 status and intussusception risk in Peutz-Jeghers syndromeN Hearle, V Schumacher, F H Menko, et al.
Journal of Medical Genetics|September 6, 2005
Multiplicity in polyp count and extracolonic manifestations in 40 Dutch patients with MYH associated polyposis coli (MAP)M Nielsen, P F Franken, T H C M Reinards, et al.
Pageof 9