Search Results - Polymorphism (materials science)

Evaluating the discriminatory power of a dissolution assay for rosuvastatin calcium capsules: Solid-state properties and dissolution media by Marilene Lopes Ângelo, André Luís Morais Ruela, Anna Clara Marques Ferreira, Marcus Vinicus de Faria Ramos, Cristina Martiniano Montanari, Lucélia Magalhães da Silva, Magali Benjamim de Araújo

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Praziquantel Fifty Years on: A Comprehensive Overview of Its Solid State by Ilenia D'Abbrunzo, Giuseppe Procida, Beatrice Perissutti

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Pharmacogenetic study of pruritus induced by epidural morphine for post cesarean section analgesia by Chia-Chi Kung, Shiou-Sheng Chen, Hong-Jyh Yang, Chih-Jun Lai, Li-Kuei Chen

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Optimization of Sintering Conditions for Improvement of Mechanical Property of a-Tricalcium Phosphate Blocks by Ill Yong Kim, Jian Wen, Koichi Kikuta, Chikara Ohtsuki

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SATB2 gene variants in non-syndromic cleft lip with or without cleft palate in Indian population by Venkatesh Babu Gurramkonda, Altaf Hussain Syed, Jyotsna Murthy, Bhaskar V.K.S. Lakkakula

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DNA finger printing of S. Mutans present in the saliva of caries active children and those associated with intellectual disability - An RAPD analysis by A.R. Prabhakar, Gudla Sreeja, Saraswatthi V. Naik

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The significance of karyotyping and azoospermia factor analysis in patients with nonobstructive azoospermia or oligozoospermia by Shin-Wen Chen, Chih-Ping Chen, Schu-Rern Chern, Yu-Ling Kuo, Chien-Ling Chiu

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Sequence analysis of matK gene of Pueraria Candollei and Butea Superba and the application of PCR-RFLP genetic marker for identification by Woraluk Yodpetch

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CYP2D6 genotyping in the daily routine of a psychiatric hospital - pharmacoeconomic evaluation by A. A. Kurylev, B. V. Andreev, A. S. Kolbin, O. V. Limankin

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Paraneoplastic pemphigus: A retrospective case series in a referral center in northern Taiwan by Yung-Tsu Cho, Jung-Ting Kao, Hsiang-Jung Chen, Li-Fang Wang, Chia-Yu Chu

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http://www.ssu.ac.ir/ijrm/index.php/ijrm/article/view/1932/980 by Nadia Arabkhazaeli, Kasra Ghanaat, Mohammad Bagher Hashemi-Soteh

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Irbesartan desmotropes: Solid-state characterization, thermodynamic study and dissolution properties by Andrea Mariela Araya-Sibaja, Carlos Eduardo Maduro de Campos, Cinira Fandaruff, José Roberto Vega-Baudrit, Teodolito Guillén-Girón, Mirtha Navarro-Hoyos, Silvia Lucía Cuffini

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First-trimester molecular diagnosis of complete hydatidiform mole associated with dizygotic twin pregnancy conceived by intrauterine insemination by Chih-Ping Chen, Tsang-Ming Ko, Chen-Yu Chen, Tao-Yeuan Wang, Schu-Rern Chern, Yu-Ling Kuo, Wayseen Wang

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Pinpointing the short-tandem repeats alleles for ethnic inferencing in forensic identification by K-medoids approach by Yoni Fuadah Syukriani, Yuyun Hidayat

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Mosaic Trisomy 9 at Amniocentesis: Prenatal Diagnosis and Molecular Genetic Analyses by Chih-Ping Chen, Hsien-Ming Lin, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Yu-Ting Chen, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang

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Mutation analysis of exon1 of bone morphogenetic protein-15 gene in Iranian patients with polycystic ovarian syndrome by Anahita Mehdizadeh, Mohammad Hasan Sheikhha, Seyed Mehdi Kalantar, Bibi Shahnaz Aali, Azam Ghanei

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Chromosome 1p36 Deletion Syndrome: Prenatal Diagnosis, Molecular Cytogenetic Characterization and Fetal Ultrasound Findings by Chih-Ping Chen, Ming Chen, Yi-Ning Su, Chin-Yuan Hsu, Fuu-Jen Tsai, Schu-Rern Chern, Pei-Chen Wu, Chen-Chi Lee, Wayseen Wang

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A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings by Chih-Ping Chen, Hsu-Kuang Huang, Pei-Ying Ling, Yi-Ning Su, Ming Chen, Fuu-Jen Tsai, Pei-Chen Wu, Schu-Rern Chern, Yu-Ting Chen, Chen-Chi Lee, Wayseen Wang

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Mosaic trisomy 2 at amniocentesis: Prenatal diagnosis and molecular genetic analysis by Chih-Ping Chen, Yi-Ning Su, Schu-Rern Chern, Yu-Ting Chen, Peih-Shan Wu, Jun-Wei Su, Chen-Wen Pan, Wayseen Wang

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Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: Prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis o... by Chih-Ping Chen, Schu-Rern Chern, Chen-Yu Chen, Pei-Chen Wu, Li-Feng Chen, Chen-Wen Pan, Wayseen Wang

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