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C Anichini

Showing results (21-30 of 32) with videos related to

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Andrologia|July 29, 2006
TEM, FISH and molecular studies in infertile men with pericentric inversion of chromosome 9G Collodel, E Moretti, S Capitani, et al.
Recenti Progressi in Medicina|March 1, 1996
[Cerebrotendinous xanthomatosis. A case report]L Sabadini, L Gonnelli, C Anichini, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|July 1, 1991
[Serum T3, T4, FT3, TSH and TBG in Turner's syndrome]C De Felice, C Anichini, R Mattei, et al.
American Journal of Medical Genetics|February 13, 2001
Exclusion of the elastin gene in the pathogenesis of Costello syndromeC Tandoi, A Botta, G Fini, et al.
American Journal of Medical Genetics. Part A|February 25, 2003
De novo double translocation 3;13 and 4;8;18 in a patient with mental retardation and skeletal abnormalitiesC Battisti, M C Bonaglia, S Giglio, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|July 1, 1991
[Correlations between individual and familial variables in Turner's syndrome]C Anichini, C De Felice, R Mattei, et al.
Human Genetics|May 1, 1993
Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to YqB Bardoni, G Floridia, S Guioli, et al.
American Journal of Medical Genetics. Part A|December 31, 2003
Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity?S Grosso, L De Cosmo, E Bonifazi, et al.
Clinical Genetics|April 26, 2008
FBN1 mutation screening of patients with Marfan syndrome and related disorders: detection of 46 novel FBN1 mutationsM Attanasio, I Lapini, L Evangelisti, et al.
Journal of Medical Genetics|February 4, 2005
Spastic paraparesis, cerebellar ataxia, and intention tremor: a severe variant of FXTAS?S Jacquemont, A Orrico, L Galli, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Andrologia|July 29, 2006
TEM, FISH and molecular studies in infertile men with pericentric inversion of chromosome 9G Collodel, E Moretti, S Capitani, et al.
Recenti Progressi in Medicina|March 1, 1996
[Cerebrotendinous xanthomatosis. A case report]L Sabadini, L Gonnelli, C Anichini, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|July 1, 1991
[Serum T3, T4, FT3, TSH and TBG in Turner's syndrome]C De Felice, C Anichini, R Mattei, et al.
American Journal of Medical Genetics|February 13, 2001
Exclusion of the elastin gene in the pathogenesis of Costello syndromeC Tandoi, A Botta, G Fini, et al.
American Journal of Medical Genetics. Part A|February 25, 2003
De novo double translocation 3;13 and 4;8;18 in a patient with mental retardation and skeletal abnormalitiesC Battisti, M C Bonaglia, S Giglio, et al.
Bollettino Della Societa Italiana Di Biologia Sperimentale|July 1, 1991
[Correlations between individual and familial variables in Turner's syndrome]C Anichini, C De Felice, R Mattei, et al.
Human Genetics|May 1, 1993
Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to YqB Bardoni, G Floridia, S Guioli, et al.
American Journal of Medical Genetics. Part A|December 31, 2003
Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity?S Grosso, L De Cosmo, E Bonifazi, et al.
Clinical Genetics|April 26, 2008
FBN1 mutation screening of patients with Marfan syndrome and related disorders: detection of 46 novel FBN1 mutationsM Attanasio, I Lapini, L Evangelisti, et al.
Journal of Medical Genetics|February 4, 2005
Spastic paraparesis, cerebellar ataxia, and intention tremor: a severe variant of FXTAS?S Jacquemont, A Orrico, L Galli, et al.
Pageof 4