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Search Results for: Hereditary Genetics
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Umbilical cord PUFA are determined by maternal and child fatty acid desaturase (FADS) genetic variants in the Avon Longitudinal Study of Parents and Children (ALSPAC)
The role of functionally defective rare germline variants of sialic acid acetylesterase (SIAE) in autoimmune Addison’s disease
Single-nucleotide polymorphisms for high-throughput genotyping of Anopheles arabiensis in East and Southern Africa
Smoking, F2RL3 methylation, and prognosis in stable coronary heart disease
Genome-Wide Association Study Identifies Novel Loci Associated with Serum Level of Vitamin B12 in Chinese Men
Gene variations in sex hormone pathways and the risk of testicular germ cell tumour: a case-parent triad study in a Norwegian-Swedish population
Effect of IL12A and IL12B polymorphisms on the risk of Chlamydia trachomatis-induced tubal factor infertility and disease severity
No evidence for genetic association with the let-7 microRNA-binding site or other common KRAS variants in risk of endometriosis
Association of melanocortin-4 receptor gene polymorphisms with obesity-related parameters in Malaysian Malays
CLOCK, PER2 and BMAL1 DNA Methylation: Association with Obesity and Metabolic Syndrome Characteristics and Monounsaturated Fat Intake
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