PDF) Clinical, phenotypic and genetic landscape of case reports with genetically proven inherited disorders of vitamin B12 metabolism: A meta-analysis
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PDF) Newborn Screening for Methylmalonic Acidemia in a Chinese Population: Molecular Genetic Confirmation and Genotype Phenotype Correlations
Full article: Vitamin B12 status in health and disease: a critical review. Diagnosis of deficiency and insufficiency – clinical and laboratory pitfalls

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Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters

PDF) Clinical, phenotypic and genetic landscape of case reports with genetically proven inherited disorders of vitamin B12 metabolism: A meta-analysis

Mechanisms of ageing: growth hormone, dietary restriction, and metformin - The Lancet Diabetes & Endocrinology

Fetal Programming by Methyl Donor Deficiency Produces Pathological Remodeling of the Ascending Aorta

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Abderrahim OUSSALAH, MCU-PH, MD, PhD, INSERM U954

Towards personalized genome-scale modeling of inborn errors of metabolism for systems medicine applications - ScienceDirect

Fetal Programming by Methyl Donor Deficiency Produces Pathological Remodeling of the Ascending Aorta
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