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M Bertoli

Showing results (81-90 of 168) with videos related to

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Human Reproduction (Oxford, England)|August 12, 2008
A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locusR A Oldenburg, M F van Dooren, B de Graaf, et al.
Clinical and Experimental Rheumatology|June 21, 2008
Adverse pregnancy outcomes in women with systemic lupus erythematosus from a multiethnic US cohort: LUMINA (LVI) [corrected]R Andrade, M L Sanchez, G S Alarcón, et al.
Pediatric Nephrology (Berlin, Germany)|January 17, 2008
A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneityMaria Luisa Conte, Aida M Bertoli-Avella, Bianca M de Graaf, et al.
European Journal of Human Genetics : EJHG|April 1, 2004
Linkage disequilibrium in young genetically isolated Dutch populationYurii S Aulchenko, Peter Heutink, Ian Mackay, et al.
European Journal of Human Genetics : EJHG|May 8, 2003
A new locus for postaxial polydactyly type A/B on chromosome 7q21-q34Robert-Jan H Galjaard, Arie P T Smits, Joep H A M Tuerlings, et al.
European Journal of Human Genetics : EJHG|December 12, 2019
Novel clinical and genetic insight into CXorf56-associated intellectual disabilityMaria Eugenia Rocha, Tainá Regina Damaceno Silveira, Erina Sasaki, et al.
Journal of Hypertension|April 13, 2004
Smoking-dependent effects of the angiotensin-converting enzyme gene insertion/deletion polymorphism on blood pressureAnna F C Schut, Fakhredin A Sayed-Tabatabaei, Jacqueline C M Witteman, et al.
Neurogenetics|December 18, 2002
A novel presenilin 1 mutation (L174 M) in a large Cuban family with early onset Alzheimer diseaseA M Bertoli Avella, B Marcheco Teruel, J J Llibre Rodriguez, et al.
American Journal of Human Genetics|August 13, 2011
Microcephaly with simplified gyration, epilepsy, and infantile diabetes linked to inappropriate apoptosis of neural progenitorsCathryn J Poulton, Rachel Schot, Sima Kheradmand Kia, et al.
Journal of Medical Genetics|July 4, 2006
A novel susceptibility locus for Hirschsprung's disease maps to 4q31.3-q32.3A S Brooks, P A Leegwater, G M Burzynski, et al.
Pageof 17

Showing results (81-90 of 168) with videos related to

Sort By:
Pageof 17
Human Reproduction (Oxford, England)|August 12, 2008
A genome-wide linkage scan in a Dutch family identifies a premature ovarian failure susceptibility locusR A Oldenburg, M F van Dooren, B de Graaf, et al.
Clinical and Experimental Rheumatology|June 21, 2008
Adverse pregnancy outcomes in women with systemic lupus erythematosus from a multiethnic US cohort: LUMINA (LVI) [corrected]R Andrade, M L Sanchez, G S Alarcón, et al.
Pediatric Nephrology (Berlin, Germany)|January 17, 2008
A genome search for primary vesicoureteral reflux shows further evidence for genetic heterogeneityMaria Luisa Conte, Aida M Bertoli-Avella, Bianca M de Graaf, et al.
European Journal of Human Genetics : EJHG|April 1, 2004
Linkage disequilibrium in young genetically isolated Dutch populationYurii S Aulchenko, Peter Heutink, Ian Mackay, et al.
European Journal of Human Genetics : EJHG|May 8, 2003
A new locus for postaxial polydactyly type A/B on chromosome 7q21-q34Robert-Jan H Galjaard, Arie P T Smits, Joep H A M Tuerlings, et al.
European Journal of Human Genetics : EJHG|December 12, 2019
Novel clinical and genetic insight into CXorf56-associated intellectual disabilityMaria Eugenia Rocha, Tainá Regina Damaceno Silveira, Erina Sasaki, et al.
Journal of Hypertension|April 13, 2004
Smoking-dependent effects of the angiotensin-converting enzyme gene insertion/deletion polymorphism on blood pressureAnna F C Schut, Fakhredin A Sayed-Tabatabaei, Jacqueline C M Witteman, et al.
Neurogenetics|December 18, 2002
A novel presenilin 1 mutation (L174 M) in a large Cuban family with early onset Alzheimer diseaseA M Bertoli Avella, B Marcheco Teruel, J J Llibre Rodriguez, et al.
American Journal of Human Genetics|August 13, 2011
Microcephaly with simplified gyration, epilepsy, and infantile diabetes linked to inappropriate apoptosis of neural progenitorsCathryn J Poulton, Rachel Schot, Sima Kheradmand Kia, et al.
Journal of Medical Genetics|July 4, 2006
A novel susceptibility locus for Hirschsprung's disease maps to 4q31.3-q32.3A S Brooks, P A Leegwater, G M Burzynski, et al.
Pageof 17