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A M Bertoli-Avella

Showing results (1-10 of 13) with videos related to

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Annals of Human Genetics|February 22, 2005
A method for pooling alleles from different genotyping experimentsY S Aulchenko, A M Bertoli-Avella, C M van Duijn
Osteoarthritis and Cartilage|March 4, 2014
Identification and analysis of a SMAD3 cis-acting eQTL operating in primary osteoarthritis and in the aneurysms and osteoarthritis syndromeE V A Raine, L N Reynard, I M B H van de Laar, et al.
Journal of Thrombosis and Haemostasis : JTH|July 15, 2010
A mutation in the acyl-coenzyme A binding domain-containing protein 5 gene (ACBD5 ) identified in autosomal dominant thrombocytopeniaF Punzo, E J Mientjes, C F Rohe, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|July 10, 2007
STOX1 gene in pre-eclampsia and intrauterine growth restrictionA L Berends, A M Bertoli-Avella, C J M de Groot, et al.
Clinical Genetics|July 31, 2018
A founder nonsense variant in NUDT2 causes a recessive neurodevelopmental disorder in Saudi Arab childrenH Yavuz, A M Bertoli-Avella, M Alfadhel, et al.
Journal of Medical Genetics|February 6, 2004
A study of gene--environment interaction on the gene for angiotensin converting enzyme: a combined functional and population based approachF A Sayed-Tabatabaei, A F C Schut, A Hofman, et al.
Journal of Medical Genetics|January 7, 2005
Angiotensin converting enzyme gene polymorphism and cardiovascular morbidity and mortality: the Rotterdam StudyF A Sayed-Tabatabaei, A F C Schut, A Arias Vásquez, et al.
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.
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.
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 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Annals of Human Genetics|February 22, 2005
A method for pooling alleles from different genotyping experimentsY S Aulchenko, A M Bertoli-Avella, C M van Duijn
Osteoarthritis and Cartilage|March 4, 2014
Identification and analysis of a SMAD3 cis-acting eQTL operating in primary osteoarthritis and in the aneurysms and osteoarthritis syndromeE V A Raine, L N Reynard, I M B H van de Laar, et al.
Journal of Thrombosis and Haemostasis : JTH|July 15, 2010
A mutation in the acyl-coenzyme A binding domain-containing protein 5 gene (ACBD5 ) identified in autosomal dominant thrombocytopeniaF Punzo, E J Mientjes, C F Rohe, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|July 10, 2007
STOX1 gene in pre-eclampsia and intrauterine growth restrictionA L Berends, A M Bertoli-Avella, C J M de Groot, et al.
Clinical Genetics|July 31, 2018
A founder nonsense variant in NUDT2 causes a recessive neurodevelopmental disorder in Saudi Arab childrenH Yavuz, A M Bertoli-Avella, M Alfadhel, et al.
Journal of Medical Genetics|February 6, 2004
A study of gene--environment interaction on the gene for angiotensin converting enzyme: a combined functional and population based approachF A Sayed-Tabatabaei, A F C Schut, A Hofman, et al.
Journal of Medical Genetics|January 7, 2005
Angiotensin converting enzyme gene polymorphism and cardiovascular morbidity and mortality: the Rotterdam StudyF A Sayed-Tabatabaei, A F C Schut, A Arias Vásquez, et al.
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.
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.
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 2