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Journal of Medical Genetics|October 1, 1981
Adenosine deaminase polymorphism. Associations at clinical level suggest a role in cell functions and immune reactionsE Bottini, E Carapella, L Cataldi, et al.Journal of Medical Genetics|December 1, 1982
Isodicentric X chromosome in a moderately tall patient with gonadal dysgenesis: lack of effect of functional centromere on inactivation patternJ Robertson, M J Faed, M A Lamont, et al.Journal of Medical Genetics|October 1, 1981
Absence of constitutive heterochromatin in a partially identified supernumerary marker chromosomeG S Pai, G H Thomas, P J BenkeJournal of Medical Genetics|April 1, 1982
Family studies on the chromosomal location of the retinoblastoma gene (Rb-1)J Morten, D G Harnden, S BundeyJournal of Medical Genetics|August 1, 1981
Genetic and clinical patterns of heritable cerebellar ataxias in adults. II. Clinical manifestationsK Kondo, K Hirota, T KatagiriJournal of Medical Genetics|August 1, 1981
Asplenia and polysplenia syndromes with abnormalities of lateralisation in a sibshipJ Zlotogora, E ElianJournal of Medical Genetics|August 1, 1981
Ring chromosome 14: a distinct clinical entityR Schmidt, L Eviatar, H M Nitowsky, et al.Journal of Medical Genetics|October 1, 1980
Ellis-van Creveld syndrome: report of 15 cases in an inbred kindredE O da Silva, D Janovitz, S C de AlbuquerqueJournal of Medical Genetics|October 1, 1980
De novo duplication 1q32-q42: variability of phenotypic features in partial lq trisomicsM S Lungarotti, A Falorni, A Calabro, et al.Journal of Medical Genetics|October 1, 1982
DHT-receptor in cultured human fibroblasts: binding study in a family with androgen insensitivity (complete testicular feminisation)E Donti, I Nicoletti, P Filipponi, et al.Pageof 649