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R Tenconi

Showing results (61-70 of 103) with videos related to

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Minerva Pediatrica|December 15, 1979
[Multinodular hepatic hemangioendothelioma in infancy. Description of 4 cases]L Zancan, G Basso, R Tenconi, et al.
Clinical Genetics|March 23, 2004
Paternal origin of LMNA mutations in Hutchinson-Gilford progeriaM R D'Apice, R Tenconi, I Mammi, et al.
Pathologica|January 1, 1983
[Reciprocal and Robertsonian translocations in a population selected for suspected chromosome anomalies]E Lenzini, L Artifoni, F Anglani, et al.
Cytogenetics and Cell Genetics|January 1, 1983
Replication patterns of human X isochromosomes by high-resolution bandingL Artifoni, C Baccichetti, E Piovan, et al.
Annales De Genetique|June 1, 1975
Partial deletion of the short arm of chromosome 12(p11; p13). Report of a caseR Tenconi, C Baccichetti, F Anglani, et al.
The New England Journal of Medicine|March 6, 1986
An inheritable anomaly of red-cell oxalate transport in "primary" calcium nephrolithiasis correctable with diureticsB Baggio, G Gambaro, F Marchini, et al.
The Journal of Pediatrics|August 1, 1984
Chorioretinal coloboma and Joubert syndrome: a nonrandom associationA M Laverda, O S Saia, P Drigo, et al.
Human Genetics|May 1, 1991
Linkage analysis of neurofibromatosis type 1. Study of a homogeneous North Italian population with five DNA markers of chromosome 17M Clementi, A Murgia, F Anglani, et al.
American Journal of Medical Genetics|March 17, 1999
Methimazole embryopathy: delineation of the phenotypeM Clementi, E Di Gianantonio, E Pelo, et al.
Human Molecular Genetics|July 1, 1993
A new disease-causing mutation in the GAP-related domain of the NF1 geneF Anglani, A Murgia, S Bedin, et al.
Pageof 11

Showing results (61-70 of 103) with videos related to

Sort By:
Pageof 11
Minerva Pediatrica|December 15, 1979
[Multinodular hepatic hemangioendothelioma in infancy. Description of 4 cases]L Zancan, G Basso, R Tenconi, et al.
Clinical Genetics|March 23, 2004
Paternal origin of LMNA mutations in Hutchinson-Gilford progeriaM R D'Apice, R Tenconi, I Mammi, et al.
Pathologica|January 1, 1983
[Reciprocal and Robertsonian translocations in a population selected for suspected chromosome anomalies]E Lenzini, L Artifoni, F Anglani, et al.
Cytogenetics and Cell Genetics|January 1, 1983
Replication patterns of human X isochromosomes by high-resolution bandingL Artifoni, C Baccichetti, E Piovan, et al.
Annales De Genetique|June 1, 1975
Partial deletion of the short arm of chromosome 12(p11; p13). Report of a caseR Tenconi, C Baccichetti, F Anglani, et al.
The New England Journal of Medicine|March 6, 1986
An inheritable anomaly of red-cell oxalate transport in "primary" calcium nephrolithiasis correctable with diureticsB Baggio, G Gambaro, F Marchini, et al.
The Journal of Pediatrics|August 1, 1984
Chorioretinal coloboma and Joubert syndrome: a nonrandom associationA M Laverda, O S Saia, P Drigo, et al.
Human Genetics|May 1, 1991
Linkage analysis of neurofibromatosis type 1. Study of a homogeneous North Italian population with five DNA markers of chromosome 17M Clementi, A Murgia, F Anglani, et al.
American Journal of Medical Genetics|March 17, 1999
Methimazole embryopathy: delineation of the phenotypeM Clementi, E Di Gianantonio, E Pelo, et al.
Human Molecular Genetics|July 1, 1993
A new disease-causing mutation in the GAP-related domain of the NF1 geneF Anglani, A Murgia, S Bedin, et al.
Pageof 11