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American Journal of Medical Genetics|May 3, 1996
Methylamine accumulation in cultured cells as a measure of the aqueous storage compartment in the laboratory diagnosis of genetic lysosomal diseasesJ Kopitz, K Harzer, A Kohlschütter, et al.American Journal of Medical Genetics|May 3, 1996
The spectrum of free neuraminic acid storage disease in childhood: clinical, morphological and biochemical observations in three non-Finnish patientsA C Sewell, C F Poets, I Degen, et al.American Journal of Medical Genetics|May 3, 1996
Differential display RT PCR of total RNA from human foreskin fibroblasts for investigation of androgen-dependent gene expressionE M Nitsche, A Moquin, P S Adams, et al.American Journal of Medical Genetics|May 3, 1996
Serial examination of 20,248 newborn fetuses and infants: correlations between drug exposure and major malformationsA Queisser-Luft, I Eggers, G Stolz, et al.American Journal of Medical Genetics|May 31, 1996
Polygenic inheritance of Tourette syndrome, stuttering, attention deficit hyperactivity, conduct, and oppositional defiant disorder: the additive and subtractive effect of the three dopaminergic genes--DRD2, D beta H, and DAT1D E Comings, S Wu, C Chiu, et al.American Journal of Medical Genetics|May 31, 1996
Allelic association but only weak evidence for linkage to the apolipoprotein E locus in late-onset Swedish Alzheimer familiesL Liu, C Forsell, L Lilius, et al.American Journal of Medical Genetics|March 3, 1997
Acampomelic campomelic dysplasia: further radiographic variationsR B Glass, K N RosenbaumAmerican Journal of Medical Genetics|March 3, 1997
Mulvihill-Smith progeria-like syndrome: a further report with delineation of phenotype, immunologic deficits, and novel observation of fibroblast abnormalitiesD C de Silva, D N Wheatley, R Herriot, et al.American Journal of Medical Genetics|March 3, 1997
Hypoplastic thymus and T-cell reduction in EECUT syndromeH Frick, D M Münger, J C Fauchère, et al.American Journal of Medical Genetics|March 3, 1997
Molecular analysis of the 5 alpha-steroid reductase type 2 gene in a family with deficiency of the enzymeF Vilchis, P Canto, B Chávez, et al.Pageof 854