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Showing results (81-90 of 89) with videos related to

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Gastroenterology|January 1, 1996
Aberrant expression of a human mucin gene (MUC5AC) in rectosigmoid villous adenomaM P Buisine, A Janin, V Maunoury, et al.
Human Genetics|April 17, 1998
Variable number tandem repeat polymorphism of the mucin genes located in the complex on 11p15.5L E Vinall, A S Hill, P Pigny, et al.
Clinical Chemistry|July 27, 2001
Heterozygous M3Mmalton alpha1-antitrypsin deficiency associated with end-stage liver disease: case report and reviewV Canva, S Piotte, J P Aubert, et al.
Annales De Chirurgie|March 24, 2005
[Paragangliomas: clinical and secretory profile. Result of 39 cases]A Lamblin, P Pigny, G Tex, et al.
Clinical Genetics|September 6, 2013
Nager syndrome: confirmation of SF3B4 haploinsufficiency as the major causeF Petit, F Escande, A S Jourdain, et al.
American Journal of Respiratory Cell and Molecular Biology|November 4, 2000
Polymorphism of human mucin genes in chest disease: possible significance of MUC2L E Vinall, J C Fowler, A L Jones, et al.
Genomics|December 15, 1996
Human mucin genes assigned to 11p15.5: identification and organization of a cluster of genesP Pigny, V Guyonnet-Duperat, A S Hill, et al.
Clinical Genetics|June 25, 2013
Split hand/foot malformation with long-bone deficiency and BHLHA9 duplication: report of 13 new familiesF Petit, A-S Jourdain, J Andrieux, et al.
American Journal of Human Genetics|July 31, 1998
Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disordersS Giraud, C X Zhang, O Serova-Sinilnikova, et al.
Pageof 9

Showing results (81-90 of 89) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 89 results.
Gastroenterology|January 1, 1996
Aberrant expression of a human mucin gene (MUC5AC) in rectosigmoid villous adenomaM P Buisine, A Janin, V Maunoury, et al.
Human Genetics|April 17, 1998
Variable number tandem repeat polymorphism of the mucin genes located in the complex on 11p15.5L E Vinall, A S Hill, P Pigny, et al.
Clinical Chemistry|July 27, 2001
Heterozygous M3Mmalton alpha1-antitrypsin deficiency associated with end-stage liver disease: case report and reviewV Canva, S Piotte, J P Aubert, et al.
Annales De Chirurgie|March 24, 2005
[Paragangliomas: clinical and secretory profile. Result of 39 cases]A Lamblin, P Pigny, G Tex, et al.
Clinical Genetics|September 6, 2013
Nager syndrome: confirmation of SF3B4 haploinsufficiency as the major causeF Petit, F Escande, A S Jourdain, et al.
American Journal of Respiratory Cell and Molecular Biology|November 4, 2000
Polymorphism of human mucin genes in chest disease: possible significance of MUC2L E Vinall, J C Fowler, A L Jones, et al.
Genomics|December 15, 1996
Human mucin genes assigned to 11p15.5: identification and organization of a cluster of genesP Pigny, V Guyonnet-Duperat, A S Hill, et al.
Clinical Genetics|June 25, 2013
Split hand/foot malformation with long-bone deficiency and BHLHA9 duplication: report of 13 new familiesF Petit, A-S Jourdain, J Andrieux, et al.
American Journal of Human Genetics|July 31, 1998
Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disordersS Giraud, C X Zhang, O Serova-Sinilnikova, et al.
Pageof 9