Unified approach to the analysis of genetic variation in serotonergic pathways

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 88, Issue 6, 1999, Pages 621-627

  Marshall, Sara E ^a   Bird, Tom G ^a   Hart, Keith ^a   Welsh, Kenneth I ^a  

^a CHURCHILL HOSPITAL   (United Kingdom)

Author keywords

Candidate gene; Complex psychiatric disease; PCR SSP; Polymorphism; Serotonin

Indexed keywords

AMINE OXIDASE (FLAVIN CONTAINING) ISOENZYME A; DNA; NUCLEOTIDE; SEROTONIN; SEROTONIN RECEPTOR; TRYPTOPHAN 2,3 DIOXYGENASE; TRYPTOPHAN HYDROXYLASE;

ARTICLE; CONTROLLED STUDY; GEL ELECTROPHORESIS; GENE; GENE FREQUENCY; GENETIC POLYMORPHISM; GENETIC VARIABILITY; HUMAN; MENTAL DISEASE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEROTONINERGIC SYSTEM;

CODON; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENE FREQUENCY; GENETIC DISEASES, INBORN; GENETIC SCREENING; HAPLOTYPES; HUMANS; INTRONS; LINKAGE DISEQUILIBRIUM; MALE; MONOAMINE OXIDASE; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RECEPTORS, SEROTONIN; SEROTONIN; TRYPTOPHAN HYDROXYLASE; TRYPTOPHAN OXYGENASE; VARIATION (GENETICS);

EID: 0033573213     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19991215)88:6<621::AID-AJMG9>3.0.CO;2-H     Document Type: Article

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