Search Results - "comparative genomics"

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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Trisomy 7 mosaicism at amniocentesis: Interphase FISH, QF-PCR, and aCGH analyses on uncultured amniocytes for rapid distinguishing of true mosaicism from pseudomosaicism by Chih-Ping Chen, Hsu-Kuang Huang, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Chen-Chi Lee, Dai-Dyi Town, Wen-Lin Chen, Yu-Ting Chen, Wayseen Wang

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Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound by Chih-Ping Chen, Shu-Yuan Chang, Yen-Ni Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Li-Feng Chen, Wayseen Wang

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Genomic Characterization of Carbapenem-Resistant Bacteria from Beef Cattle Feedlots by Sani-, Rahat Zaheer, Krysty Thomas, Sujeema Abeysekara, Travis Haight, Luke Saville, Matthew Stuart-Edwards, Athanasios Zovoilis, Tim A. McAllister

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Identification of de novo mutations for ARID1B haploinsufficiency associated with Coffin-Siris syndrome 1 in three Chinese families via array-CGH and whole exome sequencing by Guanting Lu, Qiongling Peng, Lianying Wu, Jian Zhang, Liya Ma

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Genomic profiling identifies common HPV-associated chromosomal alterations in squamous cell carcinomas of cervix and head and neck by Leemans C René, Ylstra Bauke, Meijer Gerrit A, van de Wiel Mark A, van Wieringen Wessel N, Snijders Peter JF, Smeets Serge J, Wilting Saskia M, Meijer Chris JLM, Brakenhoff Ruud H, Braakhuis Boudewijn JM, Steenbergen Renske DM

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Prenatal diagnosis of concomitant distal 5q duplication and terminal 10q deletion in a fetus with intrauterine growth restriction, congenital diaphragmatic hernia and congenital he... by Chih-Ping Chen, Jian-Pei Huang, Shin-Wen Chen, Schu-Rern Chern, Peih-Shan Wu, Fang-Tzu Wu, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang

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DNA damage and genomic instability among workers formerly and currently exposed to asbestos by Mirta Milić, Monica Neri, Marcello Ceppi, Marco Bruzzone, Armelle Munnia, Donatella Ugolini, Alfonso Cristaudo, Alessandra Bonotti, Marco E Peluso, Stefano Bonassi

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Comprehensive Genome and Plasmidome Analysis of Antimicrobial Resistant Bacteria in Wastewater Treatment Plant Effluent of Tokyo by Tsuyoshi Sekizuka, Rina Tanaka, Masanori Hashino, Koji Yatsu, Makoto Kuroda

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Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review by Chih-Ping Chen, Schu-Rern Chern, Yen-Ni Chen, Peih-Shan Wu, Chien-Wen Yang, Li-Feng Chen, Wayseen Wang

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Detection of mosaicism for 46,X,i(Y) (q10) in the blood lymphocytes in a phenotypically normal male neonate with prenatally detected 45,X/46, XY at amniocentesis and cytogenetic di... by Chih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Wen-Lin Chen, Yun-Yi Chen, Wayseen Wang

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Prenatal diagnosis of low-level mosaic trisomy 17 with maternal uniparental disomy 17 by amniocentesis in a pregnancy with a favorable outcome by Chih-Ping Chen, Shin-Yu Lin, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Wayseen Wang

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Prenatal diagnosis of maternal uniparental disomy 5 by amniocentesis associated with confined placental mosaicism for trisomy 5 and fetal trisomy 21 in a pregnancy by Chih-Ping Chen, Schu-Rern Chern, Liang-Kai Wang, Peih-Shan Wu, Fang-Tzu Wu, Yun-Yi Chen, Dai-Dyi Town, Chen-Wen Pan, Wayseen Wang

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Rapid diagnosis of pseudomosaicism in a case of Level II mosaicism for trisomy 5 in a single colony from an in situ culture of amniocytes and a review of mosaic trisomy 5 at amnioc... by Chih-Ping Chen, Shing-Jyh Chang, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chien-Wen Yang, Chen-Wen Pan, Wayseen Wang

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Recurrent fetal syndromic spina bifida associated with 3q26.1-qter duplication and 5p13.33-pter deletion due to familial balanced rearrangement by Egle Preiksaitiene, Eglė Benušienė, Zivile Ciuladaite, Vytautas Šliužas, Violeta Mikštienė, Vaidutis Kučinskas

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Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism by Chih-Ping Chen, Chris Tsai, Ming-Huei Lin, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Wen-Lin Chen, Chen-Wen Pan, Wayseen Wang

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Balanced Reciprocal Translocations Detected at Amniocentesis by Chih-Ping Chen, Pei-Chen Wu, Chen-Ju Lin, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Chen-Chi Lee, Dai-Dyi Town, Wen-Lin Chen, Li-Feng Chen, Meng-Shan Lee, Chen-Wen Pan, Wayseen Wang

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The effect of endometrial thickness on live birth outcomes in women undergoing hormone-replaced frozen embryo transfer by Rachel A. Martel, B.A, Jennifer K. Blakemore, M.D., M.Sc, James A. Grifo, M.D., Ph.D

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Detection of a familial 21q22.3 microduplication in a fetus associated with congenital heart defects by Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Tzu-Yun Chuang, Wayseen Wang

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High-level mosaicism for 45,X in 45,X/46,XX at amniocentesis in a pregnancy with a favorable outcome and postnatal progressive decrease of the 45,X cell line by Chih-Ping Chen, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Yun-Yi Chen, Wayseen Wang

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