{"id":6890,"date":"2019-10-24T15:53:16","date_gmt":"2019-10-24T13:53:16","guid":{"rendered":"https:\/\/inovie.fr\/imagenome-v2\/?page_id=6890"},"modified":"2019-10-24T15:58:39","modified_gmt":"2019-10-24T13:58:39","slug":"nos-examens","status":"publish","type":"page","link":"https:\/\/imagenome.fr\/genetique-hereditaire\/nos-examens\/","title":{"rendered":"Nos examens"},"content":{"rendered":"
Retrouvez l’ensemble de nos examens sur notre r\u00e9f\u00e9rentiel<\/strong><\/a><\/p>\nPOSTNATAL<\/h2>\n\t\t\t
Panel H\u00e9r\u00e9dit\u00e9 des cancers (13 g\u00e8nes panel HBOC)<\/a><\/h3>\n\t\t\t
BRCA1\/2 constitutionnel et somatique<\/a><\/h3>\n\t\t\t
BILHI SKIN KELOID<\/a><\/h3>\n\t\t\t
EXOME<\/a><\/h3>\n\t\t\t
Mucoviscidose : recherche cibl\u00e9e de mutation (Sanger)<\/a><\/h3>\n\t\t\t
Mucoviscidose : recherche des 51 mutations les plus fr\u00e9quentes<\/a><\/h3>\n\t\t\t
Microd\u00e9l\u00e9tion du chromosome Y<\/a><\/h3>\n\t\t\t
Mutation c.677C>T g\u00e8ne MTR<\/a><\/h3>\n\t\t\t
Mutation du facteur II<\/a><\/h3>\n\t\t\t
Mutation facteur V leiden<\/a><\/h3>\n\t\t\t
X-FRAGILE (FMR1 en Xq27.3)<\/a><\/h3>\n\t\t\t
H\u00e9mochromatose : Mutation p.Ser65Cys g\u00e8neHFE<\/a><\/h3>\n\t\t\t
H\u00e9mochromatose : Mutation p.His63Asp g\u00e8neHFE<\/a><\/h3>\n\t\t\t
H\u00e9mochromatose : Mutation p.Cys282Tyr g\u00e8neHFE<\/a><\/h3>\n\t\t\t
G\u00e9notypage HLA B27<\/a><\/h3>\n\t\t\t
HLA classe II (DQ et DR)<\/a><\/h3>\n\t\t\t
HLA classe I (A et B)<\/a><\/h3>\n\t\t\t
Analyse chromosomique (CGH)<\/a><\/h3>\n\t\t\t
PRENATAL<\/h2>\n\t\t\t
Mucoviscidose : recherche cibl\u00e9e de mutation (Sanger)<\/a><\/h3>\n\t\t\t
Mucoviscidose : recherche des 51 mutations les plus fr\u00e9quentes<\/a><\/h3>\n\t\t\t