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B Dallapiccola

Showing results (91-100 of 479) with videos related to

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Neurogenetics|May 1, 1997
A possible role of NAIP gene deletions in sex-related spinal muscular atrophy phenotype variationG Novelli, S Semprini, F Capon, et al.
Images in Paediatric Cardiology|February 28, 2012
Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-Cardio-Facial syndrome)Mc Digilio, B Marino, R Capolino, et al.
Acta Geneticae Medicae Et Gemellologiae|July 1, 1970
[Ring chromosome 18]N Ricci, B Dallapiccola, B Ventimiglia, et al.
Acta Otorhinolaryngologica Italica : Organo Ufficiale Della Societa Italiana Di Otorinolaringologia E Chirurgia Cervico-Facciale|April 1, 1996
[Genetic aspects of deafness]B Dallapiccola, R Mingarelli, M Gennarelli, et al.
Human Genetics|January 1, 1984
Premature centromere splitting in a presumptive mild form of Roberts syndromeP Petrinelli, A Antonelli, L Marcucci, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|December 1, 1987
Polymorphic DNA markers linked to cystic fibrosis locus in 20 Italian nuclear familiesG Novelli, L Potenza, A Ruzzo, et al.
La Radiologia Medica|November 1, 1978
[X-ray aspects of the trisomy 4p syndrome (proceedings)]B Dallapiccola, P P Mastroiacovo, G F Pistocchi
Pathologica|January 1, 1983
[Use of a genetic consultation service]M Frontali, G Vivona, B Dallapiccola, et al.
Journal of Neurology|January 1, 1996
Molecular basis of galactose-1-phosphate uridyltransferase deficiency involving skeletal muscleP Ninfali, N Bresolin, B Dallapiccola, et al.
International Journal of Clinical & Laboratory Research|January 1, 1996
Detection of eight beta-thalassemia mutations using a DNA enzyme immunoassayA Colosimo, G Novelli, A Cavicchini, et al.
Pageof 48

Showing results (91-100 of 479) with videos related to

Sort By:
Pageof 48
Neurogenetics|May 1, 1997
A possible role of NAIP gene deletions in sex-related spinal muscular atrophy phenotype variationG Novelli, S Semprini, F Capon, et al.
Images in Paediatric Cardiology|February 28, 2012
Clinical manifestations of Deletion 22q11.2 syndrome (DiGeorge/Velo-Cardio-Facial syndrome)Mc Digilio, B Marino, R Capolino, et al.
Acta Geneticae Medicae Et Gemellologiae|July 1, 1970
[Ring chromosome 18]N Ricci, B Dallapiccola, B Ventimiglia, et al.
Acta Otorhinolaryngologica Italica : Organo Ufficiale Della Societa Italiana Di Otorinolaringologia E Chirurgia Cervico-Facciale|April 1, 1996
[Genetic aspects of deafness]B Dallapiccola, R Mingarelli, M Gennarelli, et al.
Human Genetics|January 1, 1984
Premature centromere splitting in a presumptive mild form of Roberts syndromeP Petrinelli, A Antonelli, L Marcucci, et al.
Gene Geography : a Computerized Bulletin on Human Gene Frequencies|December 1, 1987
Polymorphic DNA markers linked to cystic fibrosis locus in 20 Italian nuclear familiesG Novelli, L Potenza, A Ruzzo, et al.
La Radiologia Medica|November 1, 1978
[X-ray aspects of the trisomy 4p syndrome (proceedings)]B Dallapiccola, P P Mastroiacovo, G F Pistocchi
Pathologica|January 1, 1983
[Use of a genetic consultation service]M Frontali, G Vivona, B Dallapiccola, et al.
Journal of Neurology|January 1, 1996
Molecular basis of galactose-1-phosphate uridyltransferase deficiency involving skeletal muscleP Ninfali, N Bresolin, B Dallapiccola, et al.
International Journal of Clinical & Laboratory Research|January 1, 1996
Detection of eight beta-thalassemia mutations using a DNA enzyme immunoassayA Colosimo, G Novelli, A Cavicchini, et al.
Pageof 48