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R Tenconi

Showing results (11-20 of 103) with videos related to

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Community Genetics|July 11, 2002
Detection of Congenital Anomalies by Fetal Ultrasonographic Examination across EuropeC. Stoll, R. Tenconi, M. Clementi
The Journal of Pediatrics|April 1, 1983
Autosomal dominant microcephalyR Tenconi, M Clementi, G Audino
American Journal of Medical Genetics|January 10, 1997
Family with branchial arch anomalies, hearing loss, ear and commissural lip pits, and rib anomalies. A new autosomal recessive condition: branchio-oto-costal syndrome?M Clementi, I Mammi, R Tenconi
Journal of Medical Genetics|April 1, 1988
Theoretical recurrence risks for cleft lip derived from a population of consecutive newbornsR Tenconi, M Clementi, L Turolla
Journal of Medical Genetics|August 1, 1990
How wide is the clinical spectrum of the acrocallosal syndrome? Report of a mild caseL Turolla, M Clementi, R Tenconi
Lancet (London, England)|December 11, 1971
Screening test for Y chromosome in newborn using urinary epithelial cellsC Baccichetti, R Tenconi, G Largaiolli
International Journal of Pediatric Otorhinolaryngology|September 1, 1981
Familial multiple pigmented naevi and sensorineural deafness. A new autosomal dominant syndrome?A Peserico, A Martini, R Tenconi
American Journal of Diseases of Children (1960)|August 1, 1972
Ultrastructure of metachromatic fibroblastsR Tenconi, C Baccichetti, E Sartouri
Human Genetics|January 1, 1990
Neurofibromatosis-1: a maximum likelihood estimation of mutation rateM Clementi, G Barbujani, L Turolla, et al.
Human Genetics|January 1, 1982
Study on segregation of the inversion of chromosome 4 (p15.2q11) in two unrelated familiesC Baccichetti, R Tenconi, D Caufin, et al.
Pageof 11

Showing results (11-20 of 103) with videos related to

Sort By:
Pageof 11
Community Genetics|July 11, 2002
Detection of Congenital Anomalies by Fetal Ultrasonographic Examination across EuropeC. Stoll, R. Tenconi, M. Clementi
The Journal of Pediatrics|April 1, 1983
Autosomal dominant microcephalyR Tenconi, M Clementi, G Audino
American Journal of Medical Genetics|January 10, 1997
Family with branchial arch anomalies, hearing loss, ear and commissural lip pits, and rib anomalies. A new autosomal recessive condition: branchio-oto-costal syndrome?M Clementi, I Mammi, R Tenconi
Journal of Medical Genetics|April 1, 1988
Theoretical recurrence risks for cleft lip derived from a population of consecutive newbornsR Tenconi, M Clementi, L Turolla
Journal of Medical Genetics|August 1, 1990
How wide is the clinical spectrum of the acrocallosal syndrome? Report of a mild caseL Turolla, M Clementi, R Tenconi
Lancet (London, England)|December 11, 1971
Screening test for Y chromosome in newborn using urinary epithelial cellsC Baccichetti, R Tenconi, G Largaiolli
International Journal of Pediatric Otorhinolaryngology|September 1, 1981
Familial multiple pigmented naevi and sensorineural deafness. A new autosomal dominant syndrome?A Peserico, A Martini, R Tenconi
American Journal of Diseases of Children (1960)|August 1, 1972
Ultrastructure of metachromatic fibroblastsR Tenconi, C Baccichetti, E Sartouri
Human Genetics|January 1, 1990
Neurofibromatosis-1: a maximum likelihood estimation of mutation rateM Clementi, G Barbujani, L Turolla, et al.
Human Genetics|January 1, 1982
Study on segregation of the inversion of chromosome 4 (p15.2q11) in two unrelated familiesC Baccichetti, R Tenconi, D Caufin, et al.
Pageof 11