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The Turkish Journal of Pediatrics
|
October 1, 1996
RFLP discordance in a PKU family due to a deletion in the PAH gene
P Bosco, N Ceratto, F Cali, et al.
Annali Di Igiene : Medicina Preventiva E Di Comunita
|
October 23, 2019
Erice 2018 Charter on the role of the National Health Service in the prevention of doping
V Romano Spica, E Di Rosa, G Savino, et al.
Human Mutation
|
April 1, 1998
Eight new mutations of the phenylalanine hydroxylase gene in Italian patients with hyperphenylalaninemia
P Bosco, F Cali, C Meli, et al.
BJU International
|
February 14, 2006
An adjustable male sling for treating urinary incontinence after prostatectomy: a phase III multicentre trial
Salomon V Romano, Sergio E Metrebian, Fernando Vaz, et al.
European Journal of Radiology
|
July 1, 1990
Gastric lymphoma: diagnosis and follow-up of chemotherapy-induced changes using real-time ultrasonography: a report of three cases
G Francica, G Cozzolino, R Morante, et al.
Human Heredity
|
October 6, 2001
Genetic heterogeneity in five Italian regions: analysis of PAH mutations and minihaplotypes
S Giannattasio, I Dianzani, P Lattanzio, et al.
Environmental Toxicology and Pharmacology
|
February 4, 2019
Microplastics occurrence in the Tyrrhenian waters and in the gastrointestinal tract of two congener species of seabreams
S Savoca, G Capillo, M Mancuso, et al.
International Journal of Legal Medicine
|
May 18, 2001
MtDNA control region and RFLP data for Sicily and France
F Cali, M G Le Roux, R D'Anna, et al.
Human Molecular Genetics
|
October 1, 1993
Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenylalaninemia in southern Europe
P Guldberg, V Romano, N Ceratto, et al.
New Biotechnology
|
November 28, 2012
The SNPs in the human genetic blueprint era
S Giampaoli, G Chillemi, F Valeriani, et al.
Page
of 21
Search research articles
Search
Showing results (151-160 of 210) with videos related to
Sort By:
Page
of 21
The Turkish Journal of Pediatrics
|
October 1, 1996
RFLP discordance in a PKU family due to a deletion in the PAH gene
P Bosco, N Ceratto, F Cali, et al.
Annali Di Igiene : Medicina Preventiva E Di Comunita
|
October 23, 2019
Erice 2018 Charter on the role of the National Health Service in the prevention of doping
V Romano Spica, E Di Rosa, G Savino, et al.
Human Mutation
|
April 1, 1998
Eight new mutations of the phenylalanine hydroxylase gene in Italian patients with hyperphenylalaninemia
P Bosco, F Cali, C Meli, et al.
BJU International
|
February 14, 2006
An adjustable male sling for treating urinary incontinence after prostatectomy: a phase III multicentre trial
Salomon V Romano, Sergio E Metrebian, Fernando Vaz, et al.
European Journal of Radiology
|
July 1, 1990
Gastric lymphoma: diagnosis and follow-up of chemotherapy-induced changes using real-time ultrasonography: a report of three cases
G Francica, G Cozzolino, R Morante, et al.
Human Heredity
|
October 6, 2001
Genetic heterogeneity in five Italian regions: analysis of PAH mutations and minihaplotypes
S Giannattasio, I Dianzani, P Lattanzio, et al.
Environmental Toxicology and Pharmacology
|
February 4, 2019
Microplastics occurrence in the Tyrrhenian waters and in the gastrointestinal tract of two congener species of seabreams
S Savoca, G Capillo, M Mancuso, et al.
International Journal of Legal Medicine
|
May 18, 2001
MtDNA control region and RFLP data for Sicily and France
F Cali, M G Le Roux, R D'Anna, et al.
Human Molecular Genetics
|
October 1, 1993
Mutational spectrum of phenylalanine hydroxylase deficiency in Sicily: implications for diagnosis of hyperphenylalaninemia in southern Europe
P Guldberg, V Romano, N Ceratto, et al.
New Biotechnology
|
November 28, 2012
The SNPs in the human genetic blueprint era
S Giampaoli, G Chillemi, F Valeriani, et al.
Page
of 21