<?xml version="1.0" encoding="UTF-8"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-10-19T01:04:31Z</responseDate><request verb="GetRecord" identifier="oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/15918" metadataPrefix="oai_dc">https://ebyu-rdlopen.rawdatalibrary.net/oai/request</request><GetRecord><record><header><identifier>oai:ebyu-rdlopen.rawdatalibrary.net:ebyu/15918</identifier><datestamp>2026-10-18T21:14:30Z</datestamp><setSpec>openaire</setSpec><setSpec>driver</setSpec><setSpec>com_ebyu_10000</setSpec><setSpec>col_ebyu_10001</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:title>Novel and rare CFTR gene mutations in Turkish patients with congenital aplasia of vas deferens</dc:title><dc:creator>Akin, Y.</dc:creator><dc:creator>Demir, D.</dc:creator><dc:creator>Görgişen, G.</dc:creator><dc:creator>Lüleci, G.</dc:creator><dc:creator>Alper, Ö. M.</dc:creator><dc:creator>Watanabe, C.S.</dc:creator><dc:creator>Sahiner, I.F.</dc:creator><dc:creator>Usta, M.F.</dc:creator><dc:subject>Cystic Fibrosis</dc:subject><dc:subject>Female</dc:subject><dc:subject>Humans</dc:subject><dc:subject>Infertility, Male</dc:subject><dc:subject>Male</dc:subject><dc:subject>Male Urogenital Diseases</dc:subject><dc:subject>Pregnancy</dc:subject><dc:subject>cystic fibrosis transmembrane conductance regulator</dc:subject><dc:subject>adult</dc:subject><dc:subject>aplasia</dc:subject><dc:subject>azoospermia</dc:subject><dc:subject>clinical article</dc:subject><dc:subject>ethnic group</dc:subject><dc:subject>gene mutation</dc:subject><dc:subject>gene sequence</dc:subject><dc:subject>genotype</dc:subject><dc:subject>human</dc:subject><dc:subject>letter</dc:subject><dc:subject>male genital tract malformation</dc:subject><dc:subject>nucleotide sequence</dc:subject><dc:subject>Turkey (republic)</dc:subject><dc:subject>vas deferens</dc:subject><dc:publisher>Blackwell Publishing Ltd</dc:publisher><dc:date>2014</dc:date><dc:type>Letter</dc:type><dc:identifier>https://rdlopen.rawdatalibrary.net/r/ebyu/15918</dc:identifier><dc:identifier>https://doi.org/10.1111/and.12053</dc:identifier><dc:identifier>0303-4569</dc:identifier><dc:language>en</dc:language><dc:relation>Andrologia</dc:relation><dc:rights>info:eu-repo/semantics/openAccess</dc:rights><dc:type>info:eu-repo/semantics/article</dc:type><dc:identifier>https://ebyu-rdlopen.rawdatalibrary.net/tr/items/ebyu/15918</dc:identifier></oai_dc:dc></metadata></record></GetRecord></OAI-PMH>