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Molecular and Cellular Probes|August 1, 1991
Precise gene dosage determination by polymerase chain reaction: theory, methodology, and statistical approachM B Lubin, J D Elashoff, S J Wang, et al.FEBS Letters|January 30, 1989
Stabilisation of cathepsin E by ATPD J Thomas, A D Richards, R A Jupp, et al.American Journal of Medical Genetics|November 1, 1982
Spondylometepiphyseal dysplasia, Strudwick typeC E Anderson, D O Sillence, R S Lachman, et al.American Journal of Medical Genetics|March 27, 1995
Bilateral ulna hypoplasia, club feet, and mental retardation: a new mesomelic syndromeG Kohn, G Malinger, R el Shawwa, et al.American Journal of Medical Genetics|February 1, 1985
Oto-palato-digital syndrome, type II--an X-linked skeletal dysplasiaT G Brewster, R S Lachman, D C Kushner, et al.Prenatal Diagnosis|May 18, 1999
Prenatal diagnosis of rhizomelic chondrodysplasia punctata due to isolated alkyldihydroacetonephosphate acyltransferase synthase deficiencyK M Brookhyser, M H Lipson, A B Moser, et al.American Journal of Medical Genetics|January 2, 1996
Epidemiology of osteochondrodysplasias: changing trends due to advances in prenatal diagnosisS A Rasmussen, F R Bieber, B R Benacerraf, et al.American Journal of Ophthalmology|February 1, 1984
Leber's congenital amaurosis associated with familial juvenile nephronophthisis and cone-shaped epiphyses of the hands (the Saldino-Mainzer syndrome)D S Ellis, J R Heckenlively, C L Martin, et al.Journal of Clinical Pathology|September 1, 1993
Serum pepsinogen I and II concentrations and IgG antibody to Helicobacter pylori in dyspeptic patientsG Biasco, G M Paganelli, D Vaira, et al.Journal of the American Geriatrics Society|November 1, 1986
Fundic atrophic gastritis in an elderly population. Effect on hemoglobin and several serum nutritional indicatorsS D Krasinski, R M Russell, I M Samloff, et al.Pageof 42