Archibald E. Garrod: The father of precision medicine

Genetics in Medicine

Volumn 18, Issue 11, 2016, Pages 1088-1089

  Perlman, Robert L ^a   Govindaraju, Diddahally R ^b  

^a UNIVERSITY OF CHICAGO   (United States)

^b ALBERT EINSTEIN COLLEGE OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HOMOGENTISIC ACID;

ACADEMIC ACHIEVEMENT; ALKAPTONURIA; AUTHOR; BOOK; CLINICAL PRACTICE; GENETIC VARIATION; HUMAN; INTROSPECTION; MEDICAL GENETICS; NOTE; PERSONALIZED MEDICINE; PHYSICIAN; SCIENTIST; CLASSIFICATION; ENGLAND; HISTORY; INBORN ERROR OF METABOLISM;

ENGLAND; HISTORY, 18TH CENTURY; HISTORY, 19TH CENTURY; HUMANS; METABOLISM, INBORN ERRORS; PHYSICIANS; PRECISION MEDICINE;

EID: 84994182367     PISSN: 10983600     EISSN: 15300366     Source Type: Journal    
DOI: 10.1038/gim.2016.5     Document Type: Note

References (7)

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2. Garrod AE. Inborn Errors of Metabolism. Henry Frowde and Hodder & Stoughton: London, 1909.
3. Garrod AE. The incidence of alkaptonuria: a study in chemical individuality. Lancet 1902;ii:1616-1620.
4. Garrod AE. The Inborn Factors in Disease: An Essay. Oxford University Press: Oxford, UK, 1931.
5. Williams RJ. Biochemical Individuality. John Wiley & Sons: New York, 1963.
6. Harris H, Hopkinson DA. Average heterozygosity per locus in man: an estimate based on the incidence of enzyme polymorphisms. Ann Hum Genet 1972;36:9-20.
7. Childs B. Genetic Medicine: A Logic of Disease. Johns Hopkins University Press: Baltimore, MD, 1999.