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Journal of Medical Genetics|April 1, 1977
Genetic heterogeneity within the chondroitinsulphaturiasB S Danes, B K Rottell, L Eviatar, et al.Journal of Medical Genetics|February 1, 1985
Increased frequency of lymphocytic mitotic non-disjunction in recurrent spontaneous abortersR C Juberg, J Knops, P N MowreyJournal of Medical Genetics|April 1, 1985
Frequency and replication status of the fragile X, fra(X)(q27-28), in a pair of monozygotic twins of markedly differing intelligenceE Tuckerman, T Webb, S E BundeyJournal of Medical Genetics|August 1, 1985
High incidence of Meckel's syndrome in Gujarati IndiansI D Young, A B Rickett, M ClarkeJournal of Medical Genetics|December 24, 1998
Mutations in the TSC1 gene account for a minority of patients with tuberous sclerosisJ B Ali, T Sepp, S Ward, et al.Journal of Medical Genetics|December 24, 1998
Genetic implications of double primary cancers of the colorectum and endometriumT Pal, T Flanders, M Mitchell-Lehman, et al.Journal of Medical Genetics|December 24, 1998
The butyrylcholinesterase K variant and susceptibility to Alzheimer's diseaseP G Kehoe, H Williams, P Holmans, et al.Journal of Medical Genetics|December 24, 1998
Costello syndrome: two cases with embryonal rhabdomyosarcomaB Kerr, O B Eden, R Dandamudi, et al.Journal of Medical Genetics|December 1, 1998
Identification of 12 novel mutations in the alpha-N-acetylglucosaminidase gene in 14 patients with Sanfilippo syndrome type B (mucopolysaccharidosis type IIIB)C E Beesley, E P Young, A Vellodi, et al.Pageof 649