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Genomics
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August 1, 1992
Localization of the human gene for carnitine palmitoyltransferase to 1p13-p11 by nonradioactive in situ hybridization
F Minoletti, I Colombo, A L Martin, et al.
The Journal of Pediatrics
|
July 1, 1996
Hypoparathyroidism in mitochondrial trifunctional protein deficiency
C Dionisi-Vici, B Garavaglia, A B Burlina, et al.
European Journal of Epidemiology
|
September 1, 1990
The nature content and interpractice variation of general practice: a regional study in Italy
F Taroni, R Stiassi, G Traversa, et al.
Genomics
|
November 1, 1994
Assignment of the human carnitine palmitoyltransferase II gene (CPT1) to chromosome 1p32
C Gellera, E Verderio, G Floridia, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
August 1, 2009
[Early nutrition: the role of genetics and epigenetics]
N Liotto, M Miozzo, M L Giannì, et al.
Journal of Inherited Metabolic Disease
|
August 13, 1998
Fumarate hydratase deficiency
E Bonioli, A Di Stefano, V Peri, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 18, 2007
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy
M Muglia, G Vazza, A Patitucci, et al.
Forensic Science International
|
October 17, 2002
Tunisian population data on 15 PCR-based loci
C Brandt-Casadevall, M Ben Dhiab, F Taroni, et al.
Forensic Science International
|
November 6, 2012
E-learning initiatives in forensic interpretation: report on experiences from current projects and outlook
A Biedermann, T Hicks, R Voisard, et al.
Annali Di Igiene : Medicina Preventiva E Di Comunita
|
March 10, 2011
[Chagas disease in a non endemic country: a study in the district of Bologna (Italy). Multidisciplinary analysis of the disease in the Latin American migrant population]
C Di Girolamo, B L Marta, A Ciannameo, et al.
Page
of 18
Search research articles
Search
Showing results (131-140 of 172) with videos related to
Sort By:
Page
of 18
Genomics
|
August 1, 1992
Localization of the human gene for carnitine palmitoyltransferase to 1p13-p11 by nonradioactive in situ hybridization
F Minoletti, I Colombo, A L Martin, et al.
The Journal of Pediatrics
|
July 1, 1996
Hypoparathyroidism in mitochondrial trifunctional protein deficiency
C Dionisi-Vici, B Garavaglia, A B Burlina, et al.
European Journal of Epidemiology
|
September 1, 1990
The nature content and interpractice variation of general practice: a regional study in Italy
F Taroni, R Stiassi, G Traversa, et al.
Genomics
|
November 1, 1994
Assignment of the human carnitine palmitoyltransferase II gene (CPT1) to chromosome 1p32
C Gellera, E Verderio, G Floridia, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
August 1, 2009
[Early nutrition: the role of genetics and epigenetics]
N Liotto, M Miozzo, M L Giannì, et al.
Journal of Inherited Metabolic Disease
|
August 13, 1998
Fumarate hydratase deficiency
E Bonioli, A Di Stefano, V Peri, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 18, 2007
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy
M Muglia, G Vazza, A Patitucci, et al.
Forensic Science International
|
October 17, 2002
Tunisian population data on 15 PCR-based loci
C Brandt-Casadevall, M Ben Dhiab, F Taroni, et al.
Forensic Science International
|
November 6, 2012
E-learning initiatives in forensic interpretation: report on experiences from current projects and outlook
A Biedermann, T Hicks, R Voisard, et al.
Annali Di Igiene : Medicina Preventiva E Di Comunita
|
March 10, 2011
[Chagas disease in a non endemic country: a study in the district of Bologna (Italy). Multidisciplinary analysis of the disease in the Latin American migrant population]
C Di Girolamo, B L Marta, A Ciannameo, et al.
Page
of 18