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Acta Neuropathologica|January 1, 1992
Autopsy findings in two siblings with infantile Refsum diseaseC W Chow, A Poulos, A J Fellenberg, et al.Biochemical Genetics|February 1, 1980
Altered copper metabolism in cultured cells from human Menkes' syndrome and mottled mouse mutantsJ Camakaris, D M Danks, L Ackland, et al.The American Journal of Physiology|April 1, 1989
Effect of chelators on copper metabolism and copper pools in mouse hepatocytesH J McArdle, S M Gross, I Creaser, et al.Biochemical Genetics|October 1, 1980
Genetics of mammalian phenylalanine hydroxylase system. IV. Evidence of phenylalanine hydroxylase in a cultured human hepatoma cell lineK H Choo, R G Cotton, I G Jennings, et al.Human Mutation|January 1, 1997
DNA repair characteristics and mutations in the ERCC2 DNA repair and transcription gene in a trichothiodystrophy patientK Takayama, D M Danks, E P Salazar, et al.American Journal of Medical Genetics|February 1, 1990
Geleophysic dysplasiaJ E Wraith, A Bankier, C W Chow, et al.Prenatal Diagnosis|May 1, 1995
New estimates of Down syndrome risks at chorionic villus sampling, amniocentesis, and livebirth in women of advanced maternal age from a uniquely defined populationJ L Halliday, L F Watson, J Lumley, et al.European Journal of Pediatrics|October 1, 1988
Maternal phenylketonuria: successful outcome in four pregnancies treated prior to conceptionB C Lynch, D B Pitt, T G Maddison, et al.Acta Neuropathologica|January 1, 1985
Congenital absence of pyramids and its significance in genetic diseasesC W Chow, J L Halliday, R M Anderson, et al.The Journal of Investigative Dermatology|March 1, 1996
Hairs from patients with maple syrup urine disease show a structural defect in the fiber cuticleL N Jones, D J Peet, D M Danks, et al.Pageof 17