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Molecular Genetics and Metabolism|November 7, 2025
Identification of variants of the MTR gene in patients with the cblG inborn error of cobalamin metabolism diagnosed by somatic cell complementation analysisDavid Watkins, Caitlin Zacharias, Kyana Arbabian-Urquilla, et al.
AIDS (London, England)|June 29, 2018
Costs and cost-effectiveness of HIV/noncommunicable disease integration in Africa: from theory to practiceRachel Nugent, Ruanne V Barnabas, Ilya Golovaty, et al.
BMC Cancer|January 22, 2015
Prognostic factors and treatment outcomes in patients with Small Bowel Adenocarcinoma (SBA): the Royal Marsden Hospital (RMH) experienceKhurum Khan, Clare Peckitt, Francesco Sclafani, et al.
Human Genetics|February 22, 2022
Epimutation in inherited metabolic disorders: the influence of aberrant transcription in adjacent genesJean-Louis Guéant, Youssef Siblini, Céline Chéry, et al.
Molecular Genetics and Metabolism|November 13, 2012
Late onset of symptoms in an atypical patient with the cblJ inborn error of vitamin B12 metabolism: diagnosis and novel mutation revealed by exome sequencingJaeseung C Kim, Ni-Chung Lee, Paul Wuh-Liang Hwu, et al.
Bulletin of the World Health Organization|January 7, 2020
Health-care investments for the urban populations, Bangladesh and IndiaDaphne Cn Wu, Eduardo P Banzon, Hellen Gelband, et al.
Clinical Colorectal Cancer|November 15, 2016
Attitudes of Patients With Gastrointestinal Cancers Toward Research BiopsiesSing Yu Moorcraft, Ruwaida Begum, David Cunningham, et al.
Molecular Genetics and Metabolism|October 3, 2012
High resolution melting analysis of the MMAA gene in patients with cblA and in those with undiagnosed methylmalonic aciduriaLaura Dempsey-Nunez, Margaret L Illson, Jana Kent, et al.
The Science of the Total Environment|February 11, 2018
Ecological-economic assessment of the effects of freshwater flow in the Florida Everglades on recreational fisheriesChristina Estela Brown, Mahadev G Bhat, Jennifer S Rehage, et al.
Pediatrics|January 9, 2013
Severe combined immunodeficiency resulting from mutations in MTHFD1Michael D Keller, Jaya Ganesh, Meredith Heltzer, et al.
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