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R Tenconi

Showing results (71-80 of 103) with videos related to

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Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|March 10, 2007
Inheritance of hyperbilirubinemia: evidence for a major autosomal recessive geneM Clementi, E Di Gianantonio, L Fabris, et al.
Collagen and Related Research|December 1, 1986
Aortic elastin abnormalities in osteogenesis imperfecta type III Pasquali-Ronchetti, D Quaglino, M Baccarani-Contri, et al.
BMJ (Clinical Research Ed.)|January 15, 1994
Clusters of anophthalmia. No link with benomyl in ItalyF Bianchi, A Calabro, E Calzolari, et al.
American Journal of Medical Genetics|July 23, 1998
Schwartz-Jampel syndrome type 2 and Stüve-Wiedemann syndrome: a case for "lumping"A Superti-Furga, R Tenconi, M Clementi, et al.
European Journal of Epidemiology|June 1, 1994
766 cases of oral cleft in Italy. Data from Emilia Romagna (IMER) and northeast Italy (NEI) registersM Milan, G Astolfi, S Volpato, et al.
Annales De Genetique|January 1, 1980
Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complexC Junien, C Turleau, J de Grouchy, et al.
Human Genetics|December 1, 1996
Sex differences in mutational rate and mutational mechanism in the NF1 gene in neurofibromatosis type 1 patientsC Lázaro, A Gaona, P Ainsworth, et al.
Reproductive Toxicology (Elmsford, N.Y.)|September 1, 1994
Anophthalmia and benomyl in Italy: a multicenter study based on 940,615 newbornsA Spagnolo, F Bianchi, A Calabro, et al.
The Journal of Investigative Dermatology|May 12, 2001
Novel keratin 17 mutations in pachyonychia congenita type 2F J Smith, C M Coleman, N M Bayoumy, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 14, 1999
Fibroblast growth factor receptor mutational screening in newborns affected by metopic synostosisM Tartaglia, V Bordoni, F Velardi, et al.
Pageof 11

Showing results (71-80 of 103) with videos related to

Sort By:
Pageof 11
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver|March 10, 2007
Inheritance of hyperbilirubinemia: evidence for a major autosomal recessive geneM Clementi, E Di Gianantonio, L Fabris, et al.
Collagen and Related Research|December 1, 1986
Aortic elastin abnormalities in osteogenesis imperfecta type III Pasquali-Ronchetti, D Quaglino, M Baccarani-Contri, et al.
BMJ (Clinical Research Ed.)|January 15, 1994
Clusters of anophthalmia. No link with benomyl in ItalyF Bianchi, A Calabro, E Calzolari, et al.
American Journal of Medical Genetics|July 23, 1998
Schwartz-Jampel syndrome type 2 and Stüve-Wiedemann syndrome: a case for "lumping"A Superti-Furga, R Tenconi, M Clementi, et al.
European Journal of Epidemiology|June 1, 1994
766 cases of oral cleft in Italy. Data from Emilia Romagna (IMER) and northeast Italy (NEI) registersM Milan, G Astolfi, S Volpato, et al.
Annales De Genetique|January 1, 1980
Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complexC Junien, C Turleau, J de Grouchy, et al.
Human Genetics|December 1, 1996
Sex differences in mutational rate and mutational mechanism in the NF1 gene in neurofibromatosis type 1 patientsC Lázaro, A Gaona, P Ainsworth, et al.
Reproductive Toxicology (Elmsford, N.Y.)|September 1, 1994
Anophthalmia and benomyl in Italy: a multicenter study based on 940,615 newbornsA Spagnolo, F Bianchi, A Calabro, et al.
The Journal of Investigative Dermatology|May 12, 2001
Novel keratin 17 mutations in pachyonychia congenita type 2F J Smith, C M Coleman, N M Bayoumy, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|August 14, 1999
Fibroblast growth factor receptor mutational screening in newborns affected by metopic synostosisM Tartaglia, V Bordoni, F Velardi, et al.
Pageof 11