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M M Weiss

Showing results (21-30 of 40) with videos related to

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Journal of Clinical Pathology|July 2, 2003
Comparative genomic hybridisation as a supportive tool in diagnostic pathologyM M Weiss, E J Kuipers, S G M Meuwissen, et al.
The Journal of Investigative Dermatology|September 1, 1983
The use of monoclonal antibody to keratin in human epidermal disease: alterations in immunohistochemical staining patternR A Weiss, G Y Guillet, I M Freedberg, et al.
The American Journal of Gastroenterology|November 6, 2001
Quantitative assessment of gastric corpus atrophy in subjects using omeprazole: a randomized follow-up studyN C van Grieken, G A Meijer, M M Weiss, et al.
Molecular Pathology : MP|April 5, 2000
Comparative genomic hybridisationM M Weiss, M A Hermsen, G A Meijer, et al.
Ophthalmic Genetics|November 12, 2010
A novel nonsense B3GALTL mutation confirms Peters plus syndrome in a patient with multiple malformations and Peters anomalyK Aliferis, C Marsal, V Pelletier, et al.
European Journal of Medical Genetics|October 5, 2014
A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disabilityJ M Cobben, M M Weiss, F S van Dijk, et al.
Journal of Clinical Pathology|March 29, 2001
Rapid quantitative assessment of gastric corpus atrophy in tissue sectionsN C van Grieken, M M Weiss, G A Meijer, et al.
Molecular Pathology : MP|September 30, 2003
Genome wide array comparative genomic hybridisation analysis of premalignant lesions of the stomachM M Weiss, E J Kuipers, C Postma, et al.
Neurology|November 29, 2008
Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotypeB F L van Nuenen, M M Weiss, B R Bloem, et al.
Clinical Genetics|May 11, 2007
Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposisM Nielsen, F J Hes, F M Nagengast, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
Journal of Clinical Pathology|July 2, 2003
Comparative genomic hybridisation as a supportive tool in diagnostic pathologyM M Weiss, E J Kuipers, S G M Meuwissen, et al.
The Journal of Investigative Dermatology|September 1, 1983
The use of monoclonal antibody to keratin in human epidermal disease: alterations in immunohistochemical staining patternR A Weiss, G Y Guillet, I M Freedberg, et al.
The American Journal of Gastroenterology|November 6, 2001
Quantitative assessment of gastric corpus atrophy in subjects using omeprazole: a randomized follow-up studyN C van Grieken, G A Meijer, M M Weiss, et al.
Molecular Pathology : MP|April 5, 2000
Comparative genomic hybridisationM M Weiss, M A Hermsen, G A Meijer, et al.
Ophthalmic Genetics|November 12, 2010
A novel nonsense B3GALTL mutation confirms Peters plus syndrome in a patient with multiple malformations and Peters anomalyK Aliferis, C Marsal, V Pelletier, et al.
European Journal of Medical Genetics|October 5, 2014
A de novo mutation in ZMYND11, a candidate gene for 10p15.3 deletion syndrome, is associated with syndromic intellectual disabilityJ M Cobben, M M Weiss, F S van Dijk, et al.
Journal of Clinical Pathology|March 29, 2001
Rapid quantitative assessment of gastric corpus atrophy in tissue sectionsN C van Grieken, M M Weiss, G A Meijer, et al.
Molecular Pathology : MP|September 30, 2003
Genome wide array comparative genomic hybridisation analysis of premalignant lesions of the stomachM M Weiss, E J Kuipers, C Postma, et al.
Neurology|November 29, 2008
Heterozygous carriers of a Parkin or PINK1 mutation share a common functional endophenotypeB F L van Nuenen, M M Weiss, B R Bloem, et al.
Clinical Genetics|May 11, 2007
Germline mutations in APC and MUTYH are responsible for the majority of families with attenuated familial adenomatous polyposisM Nielsen, F J Hes, F M Nagengast, et al.
Pageof 4