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C Petit

Showing results (401-410 of 563) with videos related to

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Human Molecular Genetics|September 25, 1997
Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY femalesK Schiebel, M Winkelmann, A Mertz, et al.
Cancer Radiotherapie : Journal De La Societe Francaise De Radiotherapie Oncologique|March 22, 2003
[Brachytherapy in cervix cancers: development of techniques and concepts]C Haie-Méder, R de Crevoisier, P Petrow, et al.
Journal of Molecular and Cellular Cardiology|September 1, 1996
Exclusion of KCNE1 (IsK) as a candidate gene for Jervell and Lange-Nielsen syndromeF Tesson, C Donger, I Denjoy, et al.
Journal of Clinical Microbiology|December 8, 2005
Isolation of nontuberculous mycobacteria in Zambia: eight case reportsPatricia C A M Buijtels, Pieter L C Petit, Henri A Verbrugh, et al.
Travel Medicine and Infectious Disease|September 15, 2009
Early small bowel perforation and cochleovestibular impairment as rare complications of typhoid feverMarlies E van Wolfswinkel, Hakima Lahri, Pieter J Wismans, et al.
Nature|June 10, 1998
Connexin 26 gene linked to a dominant deafnessF Denoyelle, G Lina-Granade, H Plauchu, et al.
Clinical Genetics|July 25, 2000
Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolatesS Ben Arab, M Hmani, F Denoyelle, et al.
Neurobiology of Disease|July 20, 2002
Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafnessF Mirghomizadeh, M Pfister, F Apaydin, et al.
European Journal of Cancer|May 1, 1981
High dose chemotherapy and autologous bone marrow transplantation in acute leukemias, malignant lymphomas and solid tumors. A study of 23 patientsN C Gorin, R David, J Stachowiak, et al.
Human Molecular Genetics|February 9, 1999
An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21M Mustapha, D Weil, S Chardenoux, et al.
Pageof 57

Showing results (401-410 of 563) with videos related to

Sort By:
Pageof 57
Human Molecular Genetics|September 25, 1997
Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY femalesK Schiebel, M Winkelmann, A Mertz, et al.
Cancer Radiotherapie : Journal De La Societe Francaise De Radiotherapie Oncologique|March 22, 2003
[Brachytherapy in cervix cancers: development of techniques and concepts]C Haie-Méder, R de Crevoisier, P Petrow, et al.
Journal of Molecular and Cellular Cardiology|September 1, 1996
Exclusion of KCNE1 (IsK) as a candidate gene for Jervell and Lange-Nielsen syndromeF Tesson, C Donger, I Denjoy, et al.
Journal of Clinical Microbiology|December 8, 2005
Isolation of nontuberculous mycobacteria in Zambia: eight case reportsPatricia C A M Buijtels, Pieter L C Petit, Henri A Verbrugh, et al.
Travel Medicine and Infectious Disease|September 15, 2009
Early small bowel perforation and cochleovestibular impairment as rare complications of typhoid feverMarlies E van Wolfswinkel, Hakima Lahri, Pieter J Wismans, et al.
Nature|June 10, 1998
Connexin 26 gene linked to a dominant deafnessF Denoyelle, G Lina-Granade, H Plauchu, et al.
Clinical Genetics|July 25, 2000
Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolatesS Ben Arab, M Hmani, F Denoyelle, et al.
Neurobiology of Disease|July 20, 2002
Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafnessF Mirghomizadeh, M Pfister, F Apaydin, et al.
European Journal of Cancer|May 1, 1981
High dose chemotherapy and autologous bone marrow transplantation in acute leukemias, malignant lymphomas and solid tumors. A study of 23 patientsN C Gorin, R David, J Stachowiak, et al.
Human Molecular Genetics|February 9, 1999
An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21M Mustapha, D Weil, S Chardenoux, et al.
Pageof 57