Search Results - "comparative genomics"

High diversity of clinical Mycobacterium intracellulare in China revealed by whole genome sequencing by Zexuan Song, Zhi Liu, Aijing Ma, Chunfa Liu, Wencong He, Xiangjie Zeng, Yiting Wang, Ping He, Dongxin Liu, Bing Zhao, Hui Xia, Shengfen Wang, Yanlin Zhao

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Spatiotemporal Co-existence of Two Mycobacterium ulcerans Clonal Complexes in the Offin River Valley of Ghana. by Araceli Lamelas, Kobina Assan Ampah, Samuel Aboagye, Sarah Kerber, Emelia Danso, Adwoa Asante-Poku, Prince Asare, Julian Parkhill, Simon R Harris, Gerd Pluschke, Dorothy Yeboah-Manu, Katharina Röltgen

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De la observación microscópica de los cromosomas en el cariotipo a los array-CGH en el diagnóstico prenatal by Wilmar Saldarriaga-Gil

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KEYPOINTS IN INVESTIGATING THE CHILD WITH GLOBAL DEVELOPMENTAL DELAY AND INTELLECTUAL DISABILITY by Diana Barca, Nina Butoianu, Oana Tarta-Arsene, Magdalena Budisteanu, Sanda Magureanu, Dana Craiu

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Female pseudohermaphroditism in a prenatally diagnosed cloacal malformation with hydronephrosis, dilated bladder, hydrometrocolpos, and oligohydramnios by Chih-Ping Chen, Chen-Yu Chen, Jun-Wei Su, Wayseen Wang

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Chromosome 11q13 deletion syndrome by Yu-Seon Kim, Gun-Ha Kim, Jung Hye Byeon, So-Hee Eun, Baik-Lin Eun

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Successful birth of South India's first twins after preimplantation genetic screening of embryos by Priya Selvaraj, Kamala Selvaraj, Kalaichelvi Srinivasan, Mahalakshmi Sivakumar

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Genetical stability and osteogenic ability of mesenchimal stem cells on demineralized bone matrices by A. Pozzuoli, C. Gardin, R. Aldegheri, E. Bressan, M. Isola, J. L. Calvo-Guirado, C. Biz, P. Arrigoni, L. Feroni, B. Zavan

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Heterozygous Deletion of Chromosome 15q13.3 in a Boy with Developmental Regression, Global Developmental Delay, Hypotonia, and Short Stature by Allison M. Strauss, Anna C. Buhle, David M. Finkler

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De la observación microscópica de los cromosomas en el cariotipo a los array-CGH en el diagnóstico prenatal by Wilmar Saldarriaga-Gil

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Successful Oocyte Retrieval, Fertilization, and Clinical Pregnancy with Low Serum β-hCG on the Day of Oocyte Collection: A Reappraisal of the Definition of the Empty Follicle Syndr... by Nicole A. Van De Velde, Charalampos Chatzicharalampous, Awoniyi O. Awonuga

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Actinobacteria in Special and Extreme Habitats: Diversity; Function Roles and Environmental Adaptations by Sheng Qin

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Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature review by Chih-Ping Chen, Ming-Chao Huang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Tzu-Yun Chuang, Dai-Dyi Town, Wayseen Wang

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Whole-genome sequencing and analysis of the Chinese herbal plant Gelsemium elegans by Yisong Liu, Qi Tang, Pi Cheng, Mingfei Zhu, Hui Zhang, Jiazhe Liu, Mengting Zuo, Chongyin Huang, Changqiao Wu, Zhiliang Sun, Zhaoying Liu

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A Biphasic Pleural Tumor with Features of an Epithelioid and Small Cell Mesothelioma: Morphologic and Molecular Findings by Sarah Hackman, Richard D. Hammer, Lester Layfield

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Detection of hypermethylation at H19DMR at amniocentesis in a fetus with overgrowth, distended abdomen and Beckwith-Wiedemann syndrome by Chih-Ping Chen, Schu-Rern Chern, Chien-Hsing Lin, Chin-Yuan Hsu, Hsiang-Yu Lin, Fang-Tzu Wu, Shin-Wen Chen, Wayseen Wang

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Mapping the landscape of tandem repeat variability by targeted long read single molecule sequencing in familial X-linked intellectual disability by Alena Zablotskaya, Hilde Van Esch, Kevin J. Verstrepen, Guy Froyen, Joris R. Vermeesch

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Perlman Syndrome with Deletion of DIS3L2 Gene by Salameh K, Viswanathan B, Nawaz Z, Habboub L, Tomerak A, Pattuvalappil R

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Next-generation Sequencing and Karyotype Analysis for the Diagnosis of Robertsonian Translocation Type Trisomy 13: A Case Report by Jing SHA, Fumin LIU, Bei ZHANG, Yang HUANG, Qinglin ZHANG, Gao JUAN, Jingfang ZHAI

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Jacobsen syndrome and neonatal bleeding: report on two unrelated patients by Gregorio Serra, Luigi Memo, Vincenzo Antona, Giovanni Corsello, Valentina Favero, Paola Lago, Mario Giuffrè

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