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Journal of Food Protection|March 28, 2019
Recovery of Fecal Coliforms and of Escherichia coli at 44.5, 45.0 and 45.5°CK F Weiss, N Chopra, P Stotland, et al.
Computer Methods in Biomechanics and Biomedical Engineering|August 18, 2022
Methodology to geometrically age human body models to average and subject-specific anthropometrics, demonstrated using a small stature female model assessed in a side impactM A Corrales, J Bolte, S Malcolm, et al.
American Journal of Medical Genetics|January 2, 1995
Proportions of spontaneous mutations in males and females with ornithine transcarbamylase deficiencyM Tuchman, I Matsuda, A Munnich, et al.
Human Genetics|February 1, 1992
Maternal origin of deletion 15q11-13 in 25/25 cases of Angelman syndromeJ C Smith, T Webb, M E Pembrey, et al.
Bone Marrow Transplantation|March 1, 1990
The use of locus-specific minisatellite probes to check engraftment following allogeneic bone marrow transplantation for severe combined immunodeficiency diseaseF Katz, S Malcolm, S Strobel, et al.
Archives of Disease in Childhood|August 1, 1989
Absence of Y specific DNA sequences in two siblings with 46XX hermaphroditismJ Raine, M E Robertson, S Malcolm, et al.
Blood|August 15, 1990
RFLP and deletion analysis for X-linked chronic granulomatous disease using the cDNA probe: potential for improved prenatal diagnosis and carrier determinationA Pelham, M A O'Reilly, S Malcolm, et al.
Southern Medical Journal|November 1, 1978
Hepatic hemangioendotheliomas and hyperbilirubinemiaG G Smith, J A Lohr, B S Malcolm, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|April 24, 2007
Directed disassembly of an interfacial rubisco protein networkSagheer A Onaizi, Andrew S Malcolm, Lizhong He, et al.
American Journal of Human Genetics|April 3, 2001
Disruption of the bipartite imprinting center in a family with Angelman syndromeK Buiting, A Barnicoat, C Lich, et al.
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