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American Journal of Medical Genetics|February 27, 2001
Distal 13q Deletion Syndrome and the VACTERL association: case report, literature review, and possible implicationsL E Walsh, G H Vance, D D WeaverAmerican Journal of Medical Genetics|February 27, 2001
Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examinationS A Irwin, B Patel, M Idupulapati, et al.American Journal of Medical Genetics|February 24, 2001
Further case of aminopterin syndrome sine aminopterin in a Spanish childS Garcia-Minaur, M P BotellaAmerican Journal of Medical Genetics|February 24, 2001
Head circumference is an independent clinical finding associated with autismJ H Miles, L L Hadden, T N Takahashi, et al.American Journal of Medical Genetics|February 24, 2001
Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxiaE Storey, D du Sart, J H Shaw, et al.American Journal of Medical Genetics|February 24, 2001
Polymorphisms at the Werner locus: II. 1074Leu/Phe, 1367Cys/Arg, longevity, and atherosclerosisE Castro, S D Edland, L Lee, et al.American Journal of Medical Genetics|February 24, 2001
Léri-Weill syndrome associated with a pseudodicentric X;Y translocation chromosome and skewed X-inactivation: implications for genetic counsellingD Baralle, L R Willatt, D J ShearsAmerican Journal of Medical Genetics|January 9, 2001
Variability in the phenotypic expression of fryns syndrome: A report of two sibshipsM Ramsing, G Gillessen-Kaesbach, W Holzgreve, et al.American Journal of Medical Genetics|January 9, 2001
Absence of 9q22-9qter in trisomy 9 does not prevent a Dandy-Walker phenotypeC S von Kaisenberg, A Caliebe, M Krams, et al.American Journal of Medical Genetics|January 9, 2001
Incidence of thrombophilia in patients with Gaucher diseaseD Elstein, P Renbaum, E Levy-Lahad, et al.Pageof 854