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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 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.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.Experientia|November 15, 1975
Ring chromosomes and leukaemiaG Alimena, L Annino, B Dallapiccola, et al.Journal of Medical Genetics|June 1, 1992
Acromegaloid facial appearance (AFA) syndrome: report of a second familyB Dallapiccola, L Zelante, L Accadia, et al.Annales De Genetique|January 1, 1989
Digeorge anomaly associated with partial deletion of chromosome 22. Report of a case with X/22 translocation and review of the literatureB Dallapiccola, B Marino, A Giannotti, et al.Human Genetics|December 15, 1976
Hand dermatoglyphics in trisomy 4pP Mastroiacovo, V Currò, A Calabro, et al.Pageof 34