Zobrazeno 1 - 1
of 1
pro vyhledávání: '"ESR2 Study Group"'
Autor:
Baetens, Dorien, Güran, Tülay, Mendonca, Berenice B., Gomes, Nathalia L., De Cauwer, Lode, Peelman, Frank, Verdin, Hannah, Vuylsteke, Marnik, Van Der Linden, Malaïka, Atay, Zeynep, Bereket, Abdullah, De Krijger, Ronald R., De Preter, Katleen, Domenice, Sorahia, Turan, Serap, Stoop, Hans, Looijenga, Leendert H., De Bosscher, Karolien, Cools, Martine, De Baere, Elfride, ESR2 Study Group
Purpose: Disorders or differences of sex development (DSDs) are rare congenital conditions characterized by atypical sex development. Despite advances in genomic technologies, the molecular cause remains unknown in 50% of cases. Methods: Homozygosity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10691::9e08aafa408ea65697da784007738057
https://dspace.library.uu.nl/handle/1874/366899
https://dspace.library.uu.nl/handle/1874/366899
