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Comparative Biochemistry and Physiology. B, Comparative Biochemistry|January 1, 1985
Changes in carnitine levels in the embryonic chick heart during developmentS A Kargas, H J Bruyere, E F Gilbert, et al.
Clinical Genetics|May 1, 1975
The evaluation of infants with the Zellweger (cerebro-hepato-renal) syndromeK W Gilchrist, E F Gilbert, N T Shahidi, et al.
Genomics|December 1, 1993
Genetic linkage of mild pseudoachondroplasia (PSACH) to markers in the pericentromeric region of chromosome 19M D Briggs, I M Rasmussen, J L Weber, et al.
The Journal of Pediatrics|December 1, 1977
Heterogeneity of nonlethal severe short-limbed dwarfismG Romeo, J Zonana, D L Rimoin, et al.
American Journal of Human Genetics|June 23, 1998
Localization of a multiple synostoses-syndrome disease gene to chromosome 17q21-22D Krakow, K Reinker, B Powell, et al.
The Journal of Pediatrics|October 1, 1978
The phenotypic variability of diastrophic dysplasiaW A Horton, D L Rimoin, R S Lachman, et al.
American Journal of Medical Genetics|December 5, 2000
Oto-palato-digital syndrome, type II: report of three cases with further delineation of the chondro-osseous morphologyR Savarirayan, V Cormier-Daire, S Unger, et al.
American Journal of Medical Genetics|July 24, 1998
Molecular, radiologic, and histopathologic correlations in thanatophoric dysplasiaW R Wilcox, P L Tavormina, D Krakow, et al.
British Journal of Pharmacology|March 1, 1996
Characterization of inositol hexakisphosphate (InsP6)-mediated priming in human neutrophils: lack of extracellular [3H]-InsP6 receptorsE Kitchen, A M Condliffe, A G Rossi, et al.
Blood|December 1, 1996
Demonstration of reversible priming of human neutrophils using platelet-activating factorE Kitchen, A G Rossi, A M Condliffe, et al.
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