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Academic Journal

ACE and AGTR1 polymorphisms in elite rhythmic gymnastics.

  • Authors : Di Cagno A; Department of Medicine and Health Sciences, University of Molise, Campobasso, Italy.; Sapere N

Subjects: Athletes* ; Gymnastics* ; Polymorphism, Genetic*

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2013 Feb; Vol. 17 (2), pp. 99-103. Date of Electronic Publication: 2012 Nov 12.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Lack of association between essential hypertension and GSTO1 uncommon genetic variants in Italian patients.

Subjects: Polymorphism, Genetic*; Glutathione Transferase/Glutathione Transferase/Glutathione Transferase/*genetics ; Hypertension/Hypertension/Hypertension/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2012 Jun; Vol. 16 (6), pp. 615-20. Date of Electronic Publication: 2012 Jan 27.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print-Electronic

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Academic Journal

Association between the ACTN3 R577X polymorphism and artistic gymnastic performance in Italy.

  • Authors : Massidda M; Department of Experimental Biology, University of Cagliari, Cagliari, Italy.; Vona G

Subjects: Athletic Performance* ; Gymnastics* ; Polymorphism, Genetic*

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2009 Jun; Vol. 13 (3), pp. 377-80.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

Serotoninergic polymorphisms (5-HTTLPR and 5-HT2A): association studies with psychosis in Alzheimer disease.

  • Authors : Rocchi A; Department of Neuroscience - Neurological Clinics, University of Pisa, Pisa, Italy.; Micheli D

Subjects: Membrane Transport Proteins* ; Polymorphism, Genetic*; Alzheimer Disease/Alzheimer Disease/Alzheimer Disease/*complications

  • Source: Genetic testing [Genet Test] 2003 Winter; Vol. 7 (4), pp. 309-14.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 9802546 Publication Model: Print Cited Medium:

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Academic Journal

Analysis of the GJB2 and GJB6 genes in Italian patients with nonsyndromic hearing loss: frequencies, novel mutations, genotypes, and degree of hearing loss.

  • Authors : Primignani P; Laboratorio di Genetica Medica, Fondazione IRCCS Ospedale Maggiore Policlinico, Mangiagalli e Regina Elena-Milano, Milan, Italy. ; Trotta L

Subjects: Genotype* ; Mutation*; Connexins/Connexins/Connexins/*genetics

  • Source: Genetic testing and molecular biomarkers [Genet Test Mol Biomarkers] 2009 Apr; Vol. 13 (2), pp. 209-17.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 101494210 Publication Model: Print Cited

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Academic Journal

Genetic analysis carried out on blood-spots of phenylalanine hydroxylase-deficient newborns detected by northeastern Italian neonatal screening.

  • Authors : Zaffanello M; Department of Paediatrics, University of Verona, 37134 Verona, Italy. ; Zamboni G

Subjects: Neonatal Screening*; DNA/DNA/DNA/*blood ; Phenylalanine Hydroxylase/Phenylalanine Hydroxylase/Phenylalanine Hydroxylase/*genetics

  • Source: Genetic testing [Genet Test] 2005 Summer; Vol. 9 (2), pp. 133-7.Publisher: Mary Ann Liebert, Inc Country of Publication: United States NLM ID: 9802546 Publication Model: Print Cited Medium:

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