Expression of the PAX2 gene in human embryos and exclusion in the CHARGE syndrome

American Journal of Medical Genetics

Volumn 93, Issue 2, 2000, Pages 85-88

  Tellier, Anne Lorraine ^a   Amiel, Jeanne ^a   Delezoide, Anne Lise ^a   Audollent, Sophie ^a   Augé, Joelle ^a   Esnault, Dominique ^a   Encha Razavi, Férechté ^a   Munnich, Arnold ^a   Lyonnet, Stanislas ^a   Vekemans, Michel ^a   Attié Bitach, Tania ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

CHARGE syndrome; Human embryos; PAX2 gene expression

Indexed keywords

ARTICLE; DNA FLANKING REGION; EMBRYO; GENE DELETION; GENE EXPRESSION; GENE LOCATION; GENE MUTATION; GENE SEQUENCE; GENE TARGETING; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC VARIABILITY; HUMAN; PRIORITY JOURNAL; SYNDROME CHARGE;

ABNORMALITIES, MULTIPLE; CENTRAL NERVOUS SYSTEM; COLOBOMA; DEAFNESS; DNA; DNA MUTATIONAL ANALYSIS; DNA-BINDING PROTEINS; EAR; EMBRYO; EXONS; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HUMANS; IN SITU HYBRIDIZATION; PAX2 TRANSCRIPTION FACTOR; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SYNDROME; TRANSCRIPTION FACTORS;

EID: 0034679911     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/1096-8628(20000717)93:2<85::AID-AJMG1>3.0.CO;2-B     Document Type: Article

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