Results 351 to 360 of about 314,978 (365)
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MENDELIAN HYPERPHENYLALANINEMIA
Annual Review of Genetics, 1988C R, Scriver, S, Kaufman, S L, Woo
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Postgraduate Medicine, 1972
The first approach to analysis of the inheritance pattern of mendelian diseases depends on whether the mutant gene or genes are located on one of the 44 (22 pairs) autosomes or on the one or two X chromosomes. No human disease is known to be associated with a mutant gene on the Y chromosome.
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The first approach to analysis of the inheritance pattern of mendelian diseases depends on whether the mutant gene or genes are located on one of the 44 (22 pairs) autosomes or on the one or two X chromosomes. No human disease is known to be associated with a mutant gene on the Y chromosome.
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Mendelian Randomization Concerns
JAMA Psychiatry, 2018Lin, Bochao Danae +2 more
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Mendelian randomization: Using genes as instruments for making causal inferences in epidemiology
Statistics in Medicine, 2008D. Lawlor +4 more
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PARITY AND MENDELIAN SEGREGATION
Journal of Heredity, 1964Strong, L C, Johnson, F N
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Mendelian forms of periodontitis
Periodontology 2000, 2007Thomas C, Hart, Jane C, Atkinson
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