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American Journal of Medical Genetics|December 1, 1991
Syndrome of developmental retardation, facial and skeletal anomalies, and hyperphosphatasia in two sisters: nosology and genetics of the Coffin-Siris syndromeP Rabe, F Haverkamp, D Emons, et al.American Journal of Medical Genetics|April 1, 1985
Familial microcephaly with normal intelligence, immunodeficiency, and risk for lymphoreticular malignancies: a new autosomal recessive disorderE Seemanová, E Passarge, D Beneskova, et al.Health Care Financing Review|February 2, 1993
Nursing home resident assessment and case-mix classification: cross-national perspectivesS B Clauser, B E FriesBMC Health Services Research|July 5, 2012
Beyond Section Q: prioritizing nursing home residents for transition to the communityBrant E Fries, Mary L JamesMedical Care|February 1, 1985
Resource utilization groups. A patient classification system for long-term careB E Fries, L M CooneyHumangenetik|July 23, 1975
Toxicity of antibiotics on cultured human skin fibroblastsW Byarugaba, H W Rüdiger, T Koske-Westphal, et al.Human Genetics|November 1, 1994
Frequency and parental origin of hypermethylated RB1 alleles in retinoblastomaV Greger, N Debus, D Lohmann, et al.Tissue Antigens|January 1, 1984
HLA-D and -DR antigens on human amniotic fluid cells. II. Heterogeneous expression of HLA-DR and other cell surface markersG Kreeb, E Valentine-Thon, K Krumbacher, et al.The Gerontologist|April 1, 2005
Elder disability as an explanation for racial differences in informal home careLydia W Li, Brant E FriesOperations Research|February 10, 1981
Determination of optimal variable-sized multiple-block appointment systemsB E Fries, V P MarathePageof 31