檢索結果 - Clayton, Joshua S.
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Multistate Mumps Outbreak Originating from Asymptomatic Transmission at a Nebraska Wedding — Six States, August–October 2019 由 Donahue, Matthew, Hendrickson, Blake, Julian, Derek, Hill, Nicholas, Rother, Julie, Koirala, Samir, Clayton, Joshua L., Safranek, Thomas, Buss, Bryan
出版 2020Text -
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Public Health Response to an Avian Influenza A(H7N8) Virus Outbreak in Commercial Turkey Flocks — Indiana, 2016 由 Brown, Jennifer A., Patel, Reema, Maitlen, Lynn, Oeding, Donna, Gordon, Karen, Clayton, Joshua L., Richards, Shawn, Pontones, Pam, Brewer, James, Blosser, Sara, Duwve, Joan
出版 2018Text -
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COVID-19 Outbreak Among Employees at a Meat Processing Facility — South Dakota, March–April 2020 由 Steinberg, Jonathan, Kennedy, Erin D., Basler, Colin, Grant, Michael P., Jacobs, Jesica R., Ortbahn, Dustin, Osburn, John, Saydah, Sharon, Tomasi, Suzanne, Clayton, Joshua L.
出版 2020Text -
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Late Vitamin K Deficiency Bleeding in Infants Whose Parents Declined Vitamin K Prophylaxis — Tennessee, 2013 由 Warren, Michael, Miller, Angela, Traylor, Julie, Sidonio, Robert, Morad, Anna, Goodman, Alyson, Christensen, Deborah, Grant, Althea, Odom, Erika, Okoroh, Ekwutosi, Clayton, Joshua, Maenner, Matthew, Marcewicz, Lauren
出版 2013Text -
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STRetch: detecting and discovering pathogenic short tandem repeat expansions 由 Dashnow, Harriet, Lek, Monkol, Phipson, Belinda, Halman, Andreas, Sadedin, Simon, Lonsdale, Andrew, Davis, Mark, Lamont, Phillipa, Clayton, Joshua S., Laing, Nigel G., MacArthur, Daniel G., Oshlack, Alicia
出版 2018Text -
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Parental Refusal of Vitamin K and Neonatal Preventive Services: A Need for Surveillance 由 Marcewicz, Lauren H., Clayton, Joshua, Maenner, Matthew, Odom, Erika, Okoroh, Ekwutosi, Christensen, Deborah, Goodman, Alyson, Warren, Michael D., Traylor, Julie, Miller, Angela, Jones, Timothy, Dunn, John, Schaffner, William, Grant, Althea
出版 2017Text -
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Regulatory Architecture of the RCA Gene Cluster Captures an Intragenic TAD Boundary, CTCF-Mediated Chromatin Looping and a Long-Range Intergenic Enhancer 由 Cheng, Jessica, Clayton, Joshua S., Acemel, Rafael D., Zheng, Ye, Taylor, Rhonda L., Keleş, Sündüz, Franke, Martin, Boackle, Susan A., Harley, John B., Quail, Elizabeth, Gómez-Skarmeta, José Luis, Ulgiati, Daniela
出版 2022Text -
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Ovine congenital progressive muscular dystrophy (OCPMD) is a model of TNNT1 congenital myopathy 由 Clayton, Joshua S., McNamara, Elyshia L., Goullee, Hayley, Conijn, Stefan, Muthsam, Keren, Musk, Gabrielle C., Coote, David, Kijas, James, Testa, Alison C., Taylor, Rhonda L., O’Hara, Amanda J., Groth, David, Ottenheijm, Coen, Ravenscroft, Gianina, Laing, Nigel G., Nowak, Kristen J.
出版 2020Text -
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Autosomal recessive cardiomyopathy and sudden cardiac death associated with variants in MYL3 由 Osborn, Daniel Peter Sayer, Emrahi, Leila, Clayton, Joshua, Tabrizi, Mehrnoush Toufan, Wan, Alex Yui Bong, Maroofian, Reza, Yazdchi, Mohammad, Garcia, Michael Leon Enrique, Galehdari, Hamid, Hesse, Camila, Shariati, Gholamreza, Mazaheri, Neda, Sedaghat, Alireza, Goullée, Hayley, Laing, Nigel, Jamshidi, Yalda, Tajsharghi, Homa
出版 2020Text -
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A novel RFC1 repeat motif (ACAGG) in two Asia-Pacific CANVAS families 由 Scriba, Carolin K, Beecroft, Sarah J, Clayton, Joshua S, Cortese, Andrea, Sullivan, Roisin, Yau, Wai Yan, Dominik, Natalia, Rodrigues, Miriam, Walker, Elizabeth, Dyer, Zoe, Wu, Teddy Y, Davis, Mark R, Chandler, David C, Weisburd, Ben, Houlden, Henry, Reilly, Mary M, Laing, Nigel G, Lamont, Phillipa J, Roxburgh, Richard H, Ravenscroft, Gianina
出版 2020Text -
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Neurogenetic fetal akinesia and arthrogryposis: genetics, expanding genotype-phenotypes and functional genomics. 由 Ravenscroft, Gianina, Clayton, Joshua S, Faiz, Fathimath, Sivadorai, Padma, Milnes, Di, Cincotta, Rob, Moon, Phillip, Kamien, Ben, Edwards, Matt, Delatycki, Martin, Lamont, Phillipa J, Chan, Sophelia HS, Colley, Alison, Ma, Alan, Collins, Felicity, Hennington, Lucinda, Zhao, Teresa, McGillivray, George, Ghedia, Sondhya, Chao, Katherine, O’Donnell-Luria, Anne, Laing, Nigel G, Davis, Mark R
出版 2020Text -
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Nebulin nemaline myopathy recapitulated in a compound heterozygous mouse model with both a missense and a nonsense mutation in Neb 由 Laitila, Jenni M., McNamara, Elyshia L., Wingate, Catherine D., Goullee, Hayley, Ross, Jacob A., Taylor, Rhonda L., van der Pijl, Robbert, Griffiths, Lisa M., Harries, Rachel, Ravenscroft, Gianina, Clayton, Joshua S., Sewry, Caroline, Lawlor, Michael W., Ottenheijm, Coen A. C., Bakker, Anthony J., Ochala, Julien, Laing, Nigel G., Wallgren-Pettersson, Carina, Pelin, Katarina, Nowak, Kristen J.
出版 2020Text