human molecular genetics
111Nature Genetics —   Titre abrégé Nature Genet. Discipline Génétique Langue Anglais Directeur de publication …
112Journal of Molecular Biology —   Titre abrégé J. Mol. Biol. Discipline Biochimie Langue Anglais Directeur de …
113Personality genetics — is a scientific field that examines the relation between personalitys and genetics.Studies investigate the link by genetic association studies where subjects are genotyped and their personality is quantified with a personality test.Among the… …
114Cooperative Human Tissue Network — The Cooperative Human Tissue Network (the CHTN) was established in 1987 by the National Cancer Institute in response to an increase in the demand for high quality biospecimens for cancer research. The purpose of the CHTN is to stimulate, for the… …
115Analysis of molecular variance — (AMOVA), is a statistical model for the molecular variation in a single species, typically biological. [Excoffier, L.; Smouse, P. E.; and Quattro, J. M. 1992. Analysis of Molecular Variance Inferred from Metric Distances among DNA Haplotypes:… …
116Corneal dystrophy (human) — Main article: corneal dystrophy Corneal dystrophy (human) Classification and external resources ICD 10 H18.5 ICD 9 …
117Institute of Molecular Pathology and Immunology of the University of Porto — The Institute of Molecular Pathology and Immunology of the University of Porto, best known by its acronym IPATIMUP ( pt. Instituto de Patologia e Imunologia Molecular da Universidade do Porto), is a Portuguese non profit institution of public… …
118Chromosome 14 (human) — Chromosome14 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 14 spans about 109 million base pairs (the building material of DNA) and represents between 3 and 3.5% of the total DNA… …
119Transition (genetics) — Not to be confused with the evolutionary concept of a transitional fossil. In genetics, a transition is a point mutation that changes a purine nucleotide to another purine (A ↔ G) or a pyrimidine nucleotide to another pyrimidine (C ↔ T).… …
120Severe combined immunodeficiency (non-human) — Severe Combined Immunodeficiency (SCID) is a severe immunodeficiency genetic disorder that is characterised by the complete inability of the adaptive immune system mount, coordinate, and sustain an appropriate immune response, usually due to… …
