Phenotypic Variability of SOCS1 Haploinsufficiency von Hale, Rebecca C., Owen, Nichole, Yuan, Bo, Chinn, Ivan K.

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Investigation of Chromosomal Structural Abnormalities in Patients With Undiagnosed Neurodevelopmental Disorders von Cao, Ye, Luk, Ho Ming, Zhang, Yanyan, Chau, Matthew Hoi Kin, Xue, Shuwen, Cheng, Shirley S W, Li, Albert Martin, Chong, Josephine S C, Leung, Tak Yeung, Dong, Zirui, Choy, Kwong Wai, Lo, Ivan Fai Man

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CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severity von Ernst, Michelle E., Baugh, Evan H., Thomas, Amanda, Bier, Louise, Lippa, Natalie, Stong, Nicholas, Mulhern, Maureen S., Kushary, Sulagna, Akman, Cigdem I., Heinzen, Erin L., Yeh, Raymond, Bi, Weimin, Hanchard, Neil A., Burrage, Lindsay C., Leduc, Magalie S., Chong, Josephine S. C., Bend, Renee, Lyons, Michael J., Lee, Jennifer A., Suwannarat, Pim, Brilstra, Eva, Simon, Marleen, Koopmans, Marije, Binsbergen, Ellen, Groepper, Daniel, Fleischer, Julie, Nava, Caroline, Keren, Boris, Mignot, Cyril, Mathieu, Sophie, Mancini, Grazia M. S., Madan‐Khetarpal, Suneeta, Infante, Elena M., Bluvstein, Judith, Seeley, Andrea, Bachman, Kristine, Klee, Eric W., Schultz‐Rogers, Laura E., Hasadsri, Linda, Barnett, Sarah, Ellingson, Marissa S., Ferber, Matthew J., Narayanan, Vinodh, Ramsey, Keri, Rauch, Anita, Joset, Pascal, Steindl, Katharina, Sheehan, Theodore, Poduri, Annapurna, Vasquez, Alejandra, Ruivenkamp, Claudia, White, Susan M., Pais, Lynn, Monaghan, Kristin G., Goldstein, David B., Sands, Tristan T., Aggarwal, Vimla

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Inherited metabolic diseases in the Southern Chinese population: spectrum of diseases and estimated incidence from recurrent mutations von Hui, Joanme, Tang, Nelson L.S., Li, C.K., Law, L.K., To, K.F., Yau, Phyllis, Fung, Simon L.M., Chong, Josephine S.C., Tsung, Lilian, Chiang, Grace, Fung, Eva, Cheung, K.L., Yeung, W.L., Fok, T.F.

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Successful Treatment of Multiple Subdural Empyemata Caused by Mycoplasma hominis in a Newborn von Chong, Josephine S.C., Tseung, Simon Y.T., Lam, Hugh S., Chu, Winnie C.W., Ip, Margaret, Wong, Hoi T., Zhu, Cannon X.L., Ng, Pak C.

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Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11 von Ravenscroft, Thomas A., Fieg, Elizabeth, Zirin, Jonathan, Kanca, Oguz, Adam, Margaret, Agrawal, Pankaj B., Alejandro, Mercedes E., Alvey, Justin, Andrews, Ashley, Azamian, Mahshid S., Bademci, Guney, Balasubramanya, Ashok, Behrens, Edward, Bican, Anna, Bohnsack, John, Botto, Lorenzo, Brown, Gabrielle, Byers, Peter, Chanprasert, Sirisak, Chao, Hsiao-Tuan, Cobban, Laurel A., Cogan, Joy D., Colley, Heather A., Cope, Heidi, Craigen, William J., Crouse, Andrew B., Dai, Hongzheng, Dayal, Jyoti G., Dipple, Katrina, Dorrani, Naghmeh, Draper, David D., Emrick, Lisa T., Falk, Marni, Fernandez, Liliana, Fieg, Elizabeth L., Findley, Laurie C., Gahl, William A., Godfrey, Rena A., Goldman, Alica M., Goldstein, David B., Hamid, Rizwan, Hanchard, Neil A., Hassey, Kelly, Hayes, Nichole, High, Frances, Hing, Anne, Hisama, Fuki M., Holm, Ingrid A., Huang, Yong, Huryn, Laryssa, Isasi, Rosario, Jarvik, Gail P., Jarvik, Jeffrey, Jayadev, Suman, Kiley, Dana, Krasnewich, Donna M., Lam, Christina, Lee, Hane, MacDowall, John, Majcherska, Marta M., Mak, Bryan C., Mamounas, Laura A., Martínez-Agosto, Julian A., McCauley, Jacob, Mulvihill, John J., Newman, John H., Oglesbee, Devin, Pace, Laura, Pallais, J. Carl, Palmer, Christina GS, Posey, Jennifer E., Potocki, Lorraine, Power, Bradley, Pusey, Barbara N., Rives, Lynette, Sacco, Ralph, Sampson, Jacinda B., Samson, Susan L., Scott, C. Ron, Schedl, Timothy, Shashi, Vandana, Tan, Queenie K.-G., Toro, Camilo, Viskochil, Dave, Wahl, Colleen E., Wambach, Jennifer, Wang, Lee-kai, Wener, Mark, Perry, Katherine Wesseling, Westerfield, Monte, Whitlock, Jordan, Yamamoto, Shinya, Yang, John, Yousef, Muhammad, Zastrow, Diane B., Zhao, Chunli, Osmond, Matthew, Postlethwait, John H., Krier, Joel, Bellen, Hugo J.

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Supply Chain Decarbonisation in Shipping and Logistics Transportation von Wong, Eugene Y. C., Lau, Henry Y. K., Chong, Josephine S. C.

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Denosumab treatment for fibrous dysplasia von Boyce, Alison M, Chong, William H, Yao, Jack, Gafni, Rachel I, Kelly, Marilyn H, Chamberlain, Christine E, Bassim, Carol, Cherman, Natasha, Ellsworth, Michelle, Kasa-Vubu, Josephine Z, Farley, Frances A, Molinolo, Alfredo A, Bhattacharyya, Nisan, Collins, Michael T

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Myosin IXa regulates epithelial differentiation and its deficiency results in hydrocephalus von Abouhamed, Marouan, Grobe, Kay, San, Isabelle V Leefa Chong, Thelen, Sabine, Honnert, Ulrike, Balda, Maria S, Matter, Karl, Bähler, Martin

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Citizen Adoption in E-Government Systems: A Meta Analysis von Olesen, Karin, Wood, Lincoln C, Chong, Josephine L. L

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Novel predictive role for mid-regional proadrenomedullin in moderate to severe aortic stenosis von Tan, Eugene S J, Oon, Yen Yee, Chan, Siew Pang, Liew, Oi Wah, Chong, Jenny P C, Tay, Edgar, Soo, Wern Miin, Yip, James W L, Gong, Lingli, Lunaria, Josephine B, Yong, Quek Wei, Lee, Evelyn Min, Yeo, Daniel P S, Ding, Zee Pin, Tang, Hak Chiaw, Ewe, See Hooi, Chin, Calvin C W, Chai, Siang Chew, Goh, Ping Ping, Ling, Lee Fong, Ong, Hean Yee, Richards, A Mark, Ling, Lieng Hsi

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Hypothermia for moderate or severe neonatal encephalopathy in low-income and middle-income countries (HELIX): a randomised controlled trial in India, Sri Lanka, and Bangladesh von Thayyil, Sudhin, Montaldo, Paolo, Shukla, Deepika, Ivain, Phoebe, Mendoza, Josephine, Moreno-Morales, Maria, Lally, Peter J, Benakappa, Naveen, Bandiya, Prathik, Somanna, Jagadish, Rajvanshi, Ankur, Jayaraman, Kumutha, Sebastian, Monica, Tamilselvam, Indumathi A, Rajendran, Usha D, Kumar, Vignesh, Vadakepat, Padmesh, Gopalan, Kavitha, Sundaram, Mangalabharathi, Seeralar, Arasar, Vinayagam, Prakash, Murugan, Kanchana D, Kumaran, Elumalai S, Mondkar, Jayashree, Manerkar, Swati, Dewang, Kapil, Bhisikar, Swapnil M, Bichkar, Vrushali, Jiwnani, Kapil, Shahidullah, Mohammod, Jahan, Ismat, Mannan, Mohammad A, Dey, Sanjoy K, Nahar, Mst N, Shabuj, Kamrul H, Abayabandara-Herath, Thilini, Chathurangika, Gayani K, Wanigasinghe, Jithangi, Sujatha, Radhika, Saraswathy, Sobhakumar, Radha, Saritha J, Krishnan, Vaisakh, Devadas, Sahana, Chandriah, Savitha, Chandrasekaran, Manigandan, Atreja, Gaurav, Muraleedharan, Pallavi, Herberg, Jethro A, Kling Chong, W K, Pressler, Ronit, Ramji, Siddarth, Shankaran, Seetha, Thayyil, Sudhin, Pant, Stuti, Shukla, Deepika, Oliveira, Vania, Ivain, Phoebe, Bassett, Paul, Swamy, Ravi, Lally, Peter J., Shivarudhrappa, Indramma, Kantharajanna, Usha B., Rajvanshi, Ankur, Joby, Poovathumkal K., Sebastian, Monica, Tamilselvam, Indumathi, Rajendran, Ushadevi, Kumar, Vignesh, Sudarsanan, Harish, Seeralar, Arasar, Vinayagam, Prakash, Sajjid, Mohamed, Murugan, Kanchana D., Sathyanathan, Babu P., Kumaran, Elumalai S., Mondkar, Jayashree, Manerkar, Swati, Joshi, Anagha R., Dewang, Kapil, Bhisikar, Swapnil M., Kalamdani, Pavan, Shahidullah, Mohammod, Moni, Sadeka C., Jahan, Ismat, Mannan, Mohammad A., Dey, Sanjoy K., Nahar, Mst. N., Islam, Mohammad N, Rodrigo, Ranmali, Chathurangika, Gayani K, Wanigasinghe, Jithangi, Saraswathy, Sobhakumar, Sarojam, Manoj K., Krishnan, Vaisakh, Nair, Mohandas K., Venkateswaran, Harini, Chandrasekaran, Manigandan, Muraleedharan, Pallavi, Pressler, Ronit, Shankaran, Seetha

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Transcriptomic convergence despite genomic divergence drive field cancerization in synchronous squamous tumors von Tan, Qiu Xuan, Shannon, Nicholas B, Lim, Weng Khong, Teo, Jing Xian, Yap, Daniel R Y, Lek, Sze Min, Tan, Joey W S, Tan, Shih Jia J, Hendrikson, Josephine, Liu, Ying, Ng, Gillian, Chong, Clara Y L, Guo, Wanyu, Koh, Kelvin K N, Ng, Cedric C Y, Rajasegaran, Vikneswari, Wong, Jolene S M, Seo, Chin Jin, Ong, Choon Kiat, Lim, Tony K H, Teh, Bin Tean, Kon, Oi Lian, Chia, Claramae S, Soo, Khee Chee, Iyer, N Gopalakrishna, Ong, Chin-Ann J

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Singapore Paediatric Resuscitation Guidelines 2021 von Ong, Gene Yong-Kwang, Ngiam, Nicola, Tham, Lai Peng, Mok, Yee Hui, Ong, Jacqueline Sm, Lee, Khai Pin, Ganapathy, Sashikumar, Chong, Shu-Ling, Pek, Jen Heng, Chew, Su Yah, Lim, Yang Chern, Shen, Germac Qiaoyue, Kua, Jade, Tan, Josephine, Ng, Kee Chong

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Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus von Anderson, Beverley H, Kasher, Paul R, Mayer, Josephine, Szynkiewicz, Marcin, Jenkinson, Emma M, Bhaskar, Sanjeev S, Urquhart, Jill E, Daly, Sarah B, Dickerson, Jonathan E, O'Sullivan, James, Leibundgut, Elisabeth Oppliger, Muter, Joanne, Abdel-Salem, Ghada M H, Babul-Hirji, Riyana, Baxter, Peter, Berger, Andrea, Bonafé, Luisa, Brunstom-Hernandez, Janice E, Buckard, Johannes A, Chitayat, David, Chong, Wui K, Cordelli, Duccio M, Ferreira, Patrick, Fluss, Joel, Forrest, Ewan H, Franzoni, Emilio, Garone, Caterina, Hammans, Simon R, Houge, Gunnar, Hughes, Imelda, Jacquemont, Sebastien, Jeannet, Pierre-Yves, Jefferson, Rosalind J, Kumar, Ram, Kutschke, Georg, Lundberg, Staffan, Lourenço, Charles M, Mehta, Ramesh, Naidu, Sakkubai, Nischal, Ken K, Nunes, Luís, Õunap, Katrin, Philippart, Michel, Prabhakar, Prab, Risen, Sarah R, Schiffmann, Raphael, Soh, Calvin, Stephenson, John B P, Stewart, Helen, Stone, Jon, Tolmie, John L, van der Knaap, Marjo S, Vieira, Jose P, Vilain, Catheline N, Wakeling, Emma L, Wermenbol, Vanessa, Whitney, Andrea, Lovell, Simon C, Meyer, Stefan, Livingston, John H, Baerlocher, Gabriela M, Black, Graeme C M, Rice, Gillian I, Crow, Yanick J

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Cognitive deficit and autism spectrum disorders: prospective diagnosis by array CGH von Nicholl, Jillian, Waters, Wendy, Mulley, John C., Suwalski, Shanna, Brown, Sue, Hull, Yvonne, Barnett, Christopher, Haan, Eric, Thompson, Elizabeth M., Liebelt, Jan, Mcgregor, Lesley, Harbord, Michael G., Entwistle, John, Munt, Chris, White, Dierdre, Chitti, Anthony, Baulderstone, David, Ketteridge, David, Friend, Kathryn, Bain, Sharon M., Sui, Y.u.

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Clinical report: a case of Williams Syndrome and Klinefelter Syndrome von Lee, Le Ye, Quek, Swee Chye, Chong, Samuel S, Tan, Arnold S C, Lum, Josephine M S, Goh, Denise Li-Meng

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