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M M Weiss

Showing results (31-40 of 40) with videos related to

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The Journal of Pathology|October 31, 2000
Helicobacter pylori-related and -non-related gastric cancers do not differ with respect to chromosomal aberrationsN C van Grieken, M M Weiss, G A Meijer, et al.
Journal of Clinical Pathology|September 1, 2006
Duodenal carcinoma in MUTYH-associated polyposisM Nielsen, J W Poley, S Verhoef, et al.
Human Mutation|January 25, 2018
Diagnostic yield of a targeted gene panel in primary ciliary dyskinesia patientsTamara Paff, Irsan E Kooi, Youssef Moutaouakil, et al.
Endocrine-Related Cancer|March 18, 2009
Pheochromocytomas and extra-adrenal paragangliomas detected by screening in patients with SDHD-associated head-and-neck paragangliomasB Havekes, A A van der Klaauw, M M Weiss, et al.
American Journal of Medical Genetics. Part A|July 3, 2007
Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndromeJuliana F Mazzeu, Ana Cristina Krepischi-Santos, Carla Rosenberg, et al.
Medchemcomm|August 16, 2018
Discovery and hit-to-lead evaluation of piperazine amides as selective, state-dependent Na<sub>V</sub>1.7 inhibitorsBrian A Sparling, S Yi, J Able, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|October 28, 2010
Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathyE Otten, R H Lekanne Dit Deprez, M M Weiss, et al.
European Journal of Medical Genetics|June 24, 2017
NGS panel analysis in 24 ectopia lentis patients; a clinically relevant test with a high diagnostic yieldE Overwater, K Floor, D van Beek, 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.
American Journal of Human Genetics|February 24, 2022
Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndromeFederico Tessadori, Karen Duran, Karen Knapp, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
The Journal of Pathology|October 31, 2000
Helicobacter pylori-related and -non-related gastric cancers do not differ with respect to chromosomal aberrationsN C van Grieken, M M Weiss, G A Meijer, et al.
Journal of Clinical Pathology|September 1, 2006
Duodenal carcinoma in MUTYH-associated polyposisM Nielsen, J W Poley, S Verhoef, et al.
Human Mutation|January 25, 2018
Diagnostic yield of a targeted gene panel in primary ciliary dyskinesia patientsTamara Paff, Irsan E Kooi, Youssef Moutaouakil, et al.
Endocrine-Related Cancer|March 18, 2009
Pheochromocytomas and extra-adrenal paragangliomas detected by screening in patients with SDHD-associated head-and-neck paragangliomasB Havekes, A A van der Klaauw, M M Weiss, et al.
American Journal of Medical Genetics. Part A|July 3, 2007
Chromosome abnormalities in two patients with features of autosomal dominant Robinow syndromeJuliana F Mazzeu, Ana Cristina Krepischi-Santos, Carla Rosenberg, et al.
Medchemcomm|August 16, 2018
Discovery and hit-to-lead evaluation of piperazine amides as selective, state-dependent Na<sub>V</sub>1.7 inhibitorsBrian A Sparling, S Yi, J Able, et al.
Netherlands Heart Journal : Monthly Journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation|October 28, 2010
Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathyE Otten, R H Lekanne Dit Deprez, M M Weiss, et al.
European Journal of Medical Genetics|June 24, 2017
NGS panel analysis in 24 ectopia lentis patients; a clinically relevant test with a high diagnostic yieldE Overwater, K Floor, D van Beek, 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.
American Journal of Human Genetics|February 24, 2022
Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndromeFederico Tessadori, Karen Duran, Karen Knapp, et al.
Pageof 4