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R Tenconi

Showing results (51-60 of 103) with videos related to

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Clinical Genetics|November 1, 1981
Chorio-retinal dysplasia, microcephaly and mental retardation. An autosomal dominant syndromeR Tenconi, M Clementi, G B Moschini, et al.
American Journal of Medical Genetics|February 11, 1997
Blastogenesis dominant 1: a sequence with midline anomalies and heterotaxyA de Meeus, P Sarda, R Tenconi, et al.
American Journal of Medical Genetics|November 1, 1991
Apparent CHARGE association and chromosome anomaly: chance or contiguous gene syndromeM Clementi, R Tenconi, L Turolla, et al.
Annales De Genetique|January 1, 1988
Partial duplication of 17 long armE Lenzini, A Leszl, L Artifoni, et al.
Journal of Maxillofacial Surgery|August 1, 1984
Popliteal pterygium syndrome presenting with orofacial abnormalities. Report of a familyG Audino, R Tenconi, M Clementi, et al.
Annales De Genetique|January 1, 1989
A new family with extra material on proximal 15qL Turolla, C Baccichetti, L Artifoni, et al.
American Journal of Medical Genetics|December 10, 1999
Neurofibromatosis type 1 growth chartsM Clementi, S Milani, I Mammi, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 1, 1996
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 geneA E Turco, M Clementi, S Rossetti, et al.
American Journal of Medical Genetics|June 1, 1986
Another Italian family with mandibuloacral dysplasia: why does it seem more frequent in Italy?R Tenconi, F Miotti, A Miotti, et al.
The British Journal of Dermatology|March 1, 1986
Pachyonychia congenita Jackson-Lawler type: a distinct malformation syndromeM Clementi, E Cardin de Stefani, C Dei Rossi, et al.
Pageof 11

Showing results (51-60 of 103) with videos related to

Sort By:
Pageof 11
Clinical Genetics|November 1, 1981
Chorio-retinal dysplasia, microcephaly and mental retardation. An autosomal dominant syndromeR Tenconi, M Clementi, G B Moschini, et al.
American Journal of Medical Genetics|February 11, 1997
Blastogenesis dominant 1: a sequence with midline anomalies and heterotaxyA de Meeus, P Sarda, R Tenconi, et al.
American Journal of Medical Genetics|November 1, 1991
Apparent CHARGE association and chromosome anomaly: chance or contiguous gene syndromeM Clementi, R Tenconi, L Turolla, et al.
Annales De Genetique|January 1, 1988
Partial duplication of 17 long armE Lenzini, A Leszl, L Artifoni, et al.
Journal of Maxillofacial Surgery|August 1, 1984
Popliteal pterygium syndrome presenting with orofacial abnormalities. Report of a familyG Audino, R Tenconi, M Clementi, et al.
Annales De Genetique|January 1, 1989
A new family with extra material on proximal 15qL Turolla, C Baccichetti, L Artifoni, et al.
American Journal of Medical Genetics|December 10, 1999
Neurofibromatosis type 1 growth chartsM Clementi, S Milani, I Mammi, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 1, 1996
An Italian family with autosomal dominant polycystic kidney disease unlinked to either the PKD1 or PKD2 geneA E Turco, M Clementi, S Rossetti, et al.
American Journal of Medical Genetics|June 1, 1986
Another Italian family with mandibuloacral dysplasia: why does it seem more frequent in Italy?R Tenconi, F Miotti, A Miotti, et al.
The British Journal of Dermatology|March 1, 1986
Pachyonychia congenita Jackson-Lawler type: a distinct malformation syndromeM Clementi, E Cardin de Stefani, C Dei Rossi, et al.
Pageof 11