Prenatal diagnosis of steroid 21-hydroxylase deficiency by allele-specific amplification

dc.contributor.author	Theodoropoulou M
dc.contributor.author	Barta, Csaba
dc.contributor.author	Szoke M
dc.contributor.author	Guttman, András
dc.contributor.author	Staub M
dc.contributor.author	Niederland T
dc.contributor.author	Sólyom, János
dc.contributor.author	Fekete, György
dc.contributor.author	Sasvári-Székely, Mária
dc.date.accessioned	2018-10-13T08:42:29Z
dc.date.available	2018-10-13T08:42:29Z
dc.date.issued	2001
dc.identifier	0034955985
dc.identifier.citation	pagination=237-240; journalVolume=16; journalIssueNumber=4; journalTitle=FETAL DIAGNOSIS AND THERAPY;
dc.identifier.uri	http://repo.lib.semmelweis.hu//handle/123456789/4998
dc.identifier.uri	doi:10.1159/000053918
dc.relation.ispartof	urn:issn:1015-3837
dc.title	Prenatal diagnosis of steroid 21-hydroxylase deficiency by allele-specific amplification
dc.type	Journal Article
dc.date.updated	2018-02-23T10:32:30Z
dc.language.rfc3066	en
dc.identifier.mtmt	19062
dc.identifier.wos	000169385500012
dc.identifier.pubmed	11399887
dc.contributor.department	SE/AOK/I/Orvosi Vegytani, Molekuláris Biológiai és Patobiokémiai Intézet
dc.contributor.department	SE/AOK/K/II. Sz. Gyermekgyógyászati Klinika
dc.contributor.institution	Semmelweis Egyetem