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Annales De Genetique|January 9, 1999
Prevalence of the C282Y mutation in Brittany: penetrance of genetic hemochromatosis?A M Jouanolle, P Fergelot, M L Raoul, et al.Annales De Genetique|January 9, 1999
A case of de novo translocation 16;21: trisomy 16q phenotype and origin of the aberrationT Eggermann, I Kolin-Gerresheim, F Gerresheim, et al.Annales De Genetique|January 1, 1991
Molecular structure of mutations at an autosomal locus in human cells: evidence for interallelic homologous recombinationJ B Little, M B BenjaminAnnales De Genetique|January 1, 1991
Bloom's syndrome in an Iranian Jewish maleC Legum, N Furman, S DiamantAnnales De Genetique|January 1, 1991
Interstitial deletion of chromosome 9q with coexistence of the deleted segment as a ring chromosome. A case reportR A Pfeiffer, U Trautmann, R Hirmer-StollAnnales De Genetique|January 1, 1991
Mosaic variegated aneuploidy with microcephaly: a new human mitotic mutant?D Warburton, K Anyane-Yeboa, P Taterka, et al.Annales De Genetique|January 1, 1988
Interaction of deletional alpha-thalassaemia with sickle cell beta-thalassaemia and its influence on foetal haemoglobin expressionD Vidaud-Raphanaud, R Krishnamoorthy, G Schaison, et al.Annales De Genetique|January 1, 1990
Hematological and biochemical studies in children with Down syndromeB Ibarra, F Rivas, C Medina, et al.Annales De Genetique|January 1, 1991
Assessment of X bends in patients with atypical X chromosome phenotypesC A Munn, S L Wenger, M W SteelePageof 129