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GENETICS / HEREDITY

Exhibiting 359 entries found in the GMN corpus.

YearTitle & TagsAuthor(s)
1652 CEIatrologismorum seu medicinalium observationum pentecostae quinque utilibus praeceptis.
1938 CEIcterus gravis (erythroblastosis) neonatorum.
1989 CEIdentification of the cystic fibrosis gene: Chromosome walking and jumping.
1989 CEIdentification of the cystic fibrosis gene: Cloning and characterization of complimentary DNA.
1989 CEIdentification of the cystic fibrosis gene: Genetic analysis.
1936 CEImmunogenetic studies of species and of species hybrids in doves, and the separation of species-specific substances in the backcross.
1985 CEIn the name of eugenics: Genetics and the uses of human heredity.
2021 CEIn vivo base editing rescues Hutchinson-Gilford progeria syndrome in mice.
1909 CEInborn errors of metabolism.
1953 CEInduction of instability at selected loci in maize.
1958 CEInfluence of light on the hyperbilirubinaemia of infants.
1933 CEInherited abnormalities of the skin and its appendages.
1883 CEInquiries into human faculty and its development.
1967 CEIntrauterine diagnosis and management of genetic defects.
1969 CEIsolation of pure lac operon DNA.
1861 CEKlinik der Leberkrankheiten. Bd. 2.
1894 CEKlinische Abbildungen: Sammlung von Darstellungen der Veränderung der äusseren Körperform bei inneren Krankheiten.
1909 CEKreuzungsuntersuchungen an Hafer und Weizen.
1965 CEKurze Geschichte der Genetik bis zur Wiederentdeckung der Vererbungsregeln Gregor Mendels. Zweite Ausgabe.
1960 CEL'opéron: Groupe de gènes à expression coordonnée par un opérateur.
1958 CEL’Hérédité en ophtalmologie.
1886 CELa syphilis héréditaire tardive.
1921 CELe bactériophage: Son rôle dans l'immunité.
1899 CELe trophoedème chronique héréditaire.
1819 CELectures on physiology, zoology and the natural history of man.
1883 CE​–1884 CELehrbuch der speciellen Pathologie und Therapie der inneren Krankheiten. 2 vols.
1959 CELes cataractes congénitales.
1904 CELes scolioses congénitales.
1519 CELiber theoricae nec non practicae Alsaharavii.
1859 CELieber das Alcapton; ein neuer Beitrag zur Frage: welche Stoffe des Harns können Kupferreduction bewirken?
1907 CELigation of the ductus arteriosus.
1990 CELinkage of early-onset familial breast cancer to Chromosome 17q21.
1994 CELocation of a breast cancer susceptibility gene, BRACA2, to chromosome 13q12-13.
1950 CELysogenicity in Escherichia coli strain K-12.
1952 CEMammalian chromosomes in vitro I: The karyotype of man.
1966 CEMan’s haemoglobins: including the haemoglobinopathies and their investigation.
1894 CEMaterials for the study of variation treated with especial regard to discontinuity in the origin of species.
1920 CEMechanismus und Physiologie der Geschlechtsbestimmung.
1936 CEMediterranean disease – thalassemia (erythroblastic anemia of Cooley); associated pigment abnormalities simulating hemochromatosis.
1884 CEMemoir upon the formation of a deaf variety of the human race.
1803 CEMemoria chirurgica sui piedi torti congenita dei fanciulli.
1902 CEMendel’s principles of heredity: A defence.
1966 CEMendelian inheritance in man; catalogs of autosomal dominant, autosomal recessive, and X-linked phenotypes.
1908 CEMendelian proportions in a mixed population.
1831 CEMerkwürdige Fragilität der Knochen ohne dyskrasische Ursache als krankhafte Eigenthümlichkeit dreier Geschwister.
1987 CEMitochondrial DNA and human evolution.
1959 CEModerne problem der humangenetik.
1968 CEMolecular pathology of human haemoglobin.
1994 CEMolecular politics: Developing American and British regulatory policy for genetic engineering, 1972-1982.
1928 CEMongolism. A study of the physical and mental characteristics of mongolian imbeciles. Revised by H. G. Brainerd.