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R Tenconi

Showing results (41-50 of 103) with videos related to

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American Journal of Medical Genetics|November 1, 1983
Ring chromosome 21 in phenotypically apparently normal persons: report of two families from Switzerland and ItalyW Schmid, R Tenconi, C Baccichetti, et al.
Human Genetics|August 1, 1997
Inheritance of cleft palate in Italy. Evidence for a major autosomal recessive locusM Clementi, R Tenconi, P Forabosco, et al.
Minerva Ginecologica|November 1, 1985
[Analysis of disaccharidase activity of the amniotic fluid for the early prenatal diagnosis of abnormalities of patency and motility of the fetal intestine]M Clementi, C Baccichetti, G Lucci, et al.
Human Genetics|November 2, 1977
Syndrome +12p. Case report and reviewR Tenconi, E Piovan, A Preto, et al.
American Journal of Medical Genetics|July 1, 1993
Is visual field reduction a component manifestation of osteopathia striata with cranial sclerosis?M Clementi, S Bellato, A Rossetti, et al.
Annales De Genetique|January 1, 1996
Clinical application of genetic polymorphism in neurofibromatosis type 1M Clementi, S Boni, I Mammi, et al.
BMJ (Clinical Research Ed.)|November 26, 1994
Amniotic band sequence in child of thalidomide victimR Tenconi, M Clementi, L Notari, et al.
Headache|January 1, 1996
Headache in patients with neurofibromatosis type 1M Clementi, P A Battistella, L Rizzi, et al.
Human Genetics|September 1, 1996
Anesthesiologic problems in Williams syndrome: the CACNL2A locus is not involvedI Mammi, D E Iles, D Smeets, et al.
American Journal of Human Genetics|August 27, 1998
Inheritance of astigmatism: evidence for a major autosomal dominant locusM Clementi, M Angi, P Forabosco, et al.
Pageof 11

Showing results (41-50 of 103) with videos related to

Sort By:
Pageof 11
American Journal of Medical Genetics|November 1, 1983
Ring chromosome 21 in phenotypically apparently normal persons: report of two families from Switzerland and ItalyW Schmid, R Tenconi, C Baccichetti, et al.
Human Genetics|August 1, 1997
Inheritance of cleft palate in Italy. Evidence for a major autosomal recessive locusM Clementi, R Tenconi, P Forabosco, et al.
Minerva Ginecologica|November 1, 1985
[Analysis of disaccharidase activity of the amniotic fluid for the early prenatal diagnosis of abnormalities of patency and motility of the fetal intestine]M Clementi, C Baccichetti, G Lucci, et al.
Human Genetics|November 2, 1977
Syndrome +12p. Case report and reviewR Tenconi, E Piovan, A Preto, et al.
American Journal of Medical Genetics|July 1, 1993
Is visual field reduction a component manifestation of osteopathia striata with cranial sclerosis?M Clementi, S Bellato, A Rossetti, et al.
Annales De Genetique|January 1, 1996
Clinical application of genetic polymorphism in neurofibromatosis type 1M Clementi, S Boni, I Mammi, et al.
BMJ (Clinical Research Ed.)|November 26, 1994
Amniotic band sequence in child of thalidomide victimR Tenconi, M Clementi, L Notari, et al.
Headache|January 1, 1996
Headache in patients with neurofibromatosis type 1M Clementi, P A Battistella, L Rizzi, et al.
Human Genetics|September 1, 1996
Anesthesiologic problems in Williams syndrome: the CACNL2A locus is not involvedI Mammi, D E Iles, D Smeets, et al.
American Journal of Human Genetics|August 27, 1998
Inheritance of astigmatism: evidence for a major autosomal dominant locusM Clementi, M Angi, P Forabosco, et al.
Pageof 11