Hasil Pencarian - Purevdorj Ichinkhorloo
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Use of Double Test Biomarkers to Predict Fetal Nuchal Translucency Thickness in the Diagnosis of Trisomy 21: A Compromise between Sensitivity and Specificity oleh Ganzug Jugder, Oyunchimeg Unshigbayar, Purevdorj Ichinkhorloo, Tsolmon Boldoo, Erkhembulgan Purev
Diterbitkan 2018-09-01Dapatkan teks lengkap
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The genetic analysis of eight families with hemophilia B in Mongolia: Identification of two novel mutation oleh Purevdorj Munkhuu, Munkhtsetseg Bazarragchaa, Purevdorj Ichinkhorloo, Ki‐Young Yoo, Enkh‐Amar Ayush, Ochbadrakh Batjargal, Erdenebayar Namjil, Sarantuya Jav, Erkhembulgan Purevdorj, Sodnomtsogt Lkhagvasuren
Diterbitkan 2024-09-01Dapatkan teks lengkap
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