Hasil Pencarian - Cynthia C. Morton

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  1. 1
    Editorial: Chromosome structural variants: Epidemiology, identification and contribution to human diseases

    Editorial: Chromosome structural variants: Epidemiology, identification and contribution to human diseases oleh Zirui Dong, Zirui Dong, Zirui Dong, Zirui Dong, Dezso David, Claudia Gonzaga-Jauregui, Cynthia C. Morton, Cynthia C. Morton, Cynthia C. Morton, Cynthia C. Morton, Cynthia C. Morton, Cinthya J. Zepeda-Mendoza

    Diterbitkan 2022-09-01
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  2. 2
    Identification and function of long non-coding RNA

    Identification and function of long non-coding RNA oleh Carl eErnst, Cynthia C Morton

    Diterbitkan 2013-10-01
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  3. 3
    Cochlin Deficiency Protects Against Noise-Induced Hearing Loss

    Cochlin Deficiency Protects Against Noise-Induced Hearing Loss oleh Richard Seist, Richard Seist, Richard Seist, Lukas D. Landegger, Lukas D. Landegger, Lukas D. Landegger, Nahid G. Robertson, Sasa Vasilijic, Sasa Vasilijic, Cynthia C. Morton, Cynthia C. Morton, Cynthia C. Morton, Cynthia C. Morton, Konstantina M. Stankovic, Konstantina M. Stankovic, Konstantina M. Stankovic, Konstantina M. Stankovic

    Diterbitkan 2021-05-01
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  4. 4
    Pelvic and pulmonary benign metastasizing leiomyoma: A case report

    Pelvic and pulmonary benign metastasizing leiomyoma: A case report oleh Jennifer B. Bakkensen, Wesley Samore, Pietro Bortoletto, Cynthia C. Morton, Raymond M. Anchan

    Diterbitkan 2018-04-01
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  5. 5
    Experience of Low-Pass Whole-Genome Sequencing-Based Copy Number Variant Analysis: A Survey of Chinese Tertiary Hospitals

    Experience of Low-Pass Whole-Genome Sequencing-Based Copy Number Variant Analysis: A Survey of Chinese Tertiary Hospitals oleh Yu Zheng, Baosheng Zhu, Jichun Tan, Yichun Guan, The Chinese Genomic Structural Variants Consortium, Cynthia C. Morton, Guangxiu Lu

    Diterbitkan 2022-04-01
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  6. 6
    Hereditary leiomyomatosis and renal cell cancer: Cutaneous lesions & atypical fibroids

    Hereditary leiomyomatosis and renal cell cancer: Cutaneous lesions & atypical fibroids oleh Pietro Bortoletto, Jennifer L. Lindsey, Liping Yuan, Bradley J. Quade, Antonio R. Gargiulo, Cynthia C. Morton, Elizabeth A. Stewart, Raymond M. Anchan

    Diterbitkan 2017-07-01
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  7. 7
    The Burden and Benefits of Knowledge: Ethical Considerations Surrounding Population-Based Newborn Genome Screening for Hearing

    The Burden and Benefits of Knowledge: Ethical Considerations Surrounding Population-Based Newborn Genome Screening for Hearing oleh Calli O. Mitchell, Greysha Rivera-Cruz, Matthew Hoi Kin Chau, Zirui Dong, Kwong Wai Choy, Jun Shen, Sami Amr, Anne B. S. Giersch, Cynthia C. Morton

    Diterbitkan 2022-05-01
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  8. 8
    Targeted insertion of conditional expression cassettes into the mouse genome using the modified i-PITT

    Targeted insertion of conditional expression cassettes into the mouse genome using the modified i-PITT oleh Hiromi Miura, Ayaka Nakamura, Aki Kurosaki, Ai Kotani, Masaru Motojima, Keiko Tanaka, Shigeru Kakuta, Sanae Ogiwara, Yuhsuke Ohmi, Hirotaka Komaba, Samantha L.P. Schilit, Cynthia C. Morton, Channabasavaiah B. Gurumurthy, Masato Ohtsuka

    Diterbitkan 2024-06-01
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  9. 9
    A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome

    A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndro... oleh Afif Ben-Mahmoud, Shotaro Kishikawa, Vijay Gupta, Natalia T. Leach, Yiping Shen, Oana Moldovan, Himanshu Goel, Bruce Hopper, Kara Ranguin, Nicolas Gruchy, Saskia M Maas, Yves Lacassie, Soo-Hyun Kim, Woo-Yang Kim, Bradley J. Quade, Cynthia C. Morton, Cheol-Hee Kim, Lawrence C. Layman, Hyung-Goo Kim

    Diterbitkan 2023-08-01
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  10. 10
    NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects.

    NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects. oleh Weining Lu, Fabiola Quintero-Rivera, Yanli Fan, Fowzan S Alkuraya, Diana J Donovan, Qiongchao Xi, Annick Turbe-Doan, Qing-Gang Li, Craig G Campbell, Alan L Shanske, Elliott H Sherr, Ayesha Ahmad, Roxana Peters, Benedict Rilliet, Paloma Parvex, Alexander G Bassuk, David J Harris, Heather Ferguson, Chantal Kelly, Christopher A Walsh, Richard M Gronostajski, Koenraad Devriendt, Anne Higgins, Azra H Ligon, Bradley J Quade, Cynthia C Morton, James F Gusella, Richard L Maas

    Diterbitkan 2007-05-01
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