Genetic diseases that are linked to gene mutations on the X CHROMOSOME in humans (X CHROMOSOME, HUMAN) or the X CHROMOSOME in other species. Included here are animal models of human X-linked diseases
Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero
Genetic disorders -- Diagnosis -- United States -- Congresses : Genome-based diagnostics : clarifying pathways to clinical use : workshop summary / Steve Olson and Adam C. Berger, rapporteurs ; Roundtable on Translating Genomic-Based Research for Health, Board on Health Sciences Policy, Institute of Medicine of the National Academies
Genetic disorders -- Diet therapy -- Congresses : Examining special nutritional requirements in disease states : proceedings of a workshop / Anne Brown Rodgers, rapporteur ; Food and Nutrition Board, Health and Medicine Division, National Academies of Sciences, Engineering, and Medicine
--subdivision Genetics under individual animals and groups of animals; and subdivision Diseases--Genetic aspects under individual animals and groups of animals, e.g. Cattle--Genetics; Cattle--Diseases--Genetic aspects
Genetic disorders in children -- United States : The student with a genetic disorder : educational implications for special education teachers and for physical therapists, occupational therapists, and speech pathologists / edited by Diane Plumridge [and others]
