Designing Virtual Reading Room (VRR Digi_Litikon) for learning batik in Vocational High Schools: Curriculum material improvement by Widiaty, I, Wahyudin, D, Abdullah, A G, Riyana, C, Mubaroq, S R

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De novo pathogenic variant in TUBB2A presenting with arthrogryposis multiplex congenita, brain abnormalities, and severe developmental delay by Ejaz, Resham, Lionel, Anath C., Blaser, Susan, Walker, Susan, Scherer, Stephen W., Babul‐Hirji, Riyana, Marshall, Christian R., Stavropoulos, Dimitri J., Chitayat, David

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From riverbank to the sea: An initial assessment of plastic pollution along the Ciliwung River, Indonesia by Cordova, Muhammad Reza, Kelly, Max R., Hafizt, Muhammad, Wibowo, Singgih Prasetyo Adi, Ulumuddin, Yaya Ihya, Purbonegoro, Triyoni, Yogaswara, Deny, Kaisupy, Muhammad Taufik, Subandi, Riyana, Sani, Sofia Yuniar, Thompson, Richard C., Jobling, Susan

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CYP26B1-related disorder: expanding the ends of the spectrum through clinical and molecular evidence by Silveira, Karina C., Fonseca, Inara Chacon, Oborn, Connor, Wengryn, Parker, Ghafoor, Saima, Beke, Alexander, Dreseris, Ema S., Wong, Cassandra, Iacovone, Aline, Soltys, Carrie-Lynn, Babul-Hirji, Riyana, Artigalas, Osvaldo, Antolini-Tavares, Arthur, Gingras, Anne-Claude, Campos, Eric, Cavalcanti, Denise P., Kannu, Peter

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Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine by Stavropoulos, Dimitri J, Merico, Daniele, Jobling, Rebekah, Bowdin, Sarah, Monfared, Nasim, Thiruvahindrapuram, Bhooma, Nalpathamkalam, Thomas, Pellecchia, Giovanna, Yuen, Ryan K C, Szego, Michael J, Hayeems, Robin Z, Shaul, Randi Zlotnik, Brudno, Michael, Girdea, Marta, Frey, Brendan, Alipanahi, Babak, Ahmed, Sohnee, Babul-Hirji, Riyana, Porras, Ramses Badilla, Carter, Melissa T, Chad, Lauren, Chaudhry, Ayeshah, Chitayat, David, Doust, Soghra Jougheh, Cytrynbaum, Cheryl, Dupuis, Lucie, Ejaz, Resham, Fishman, Leona, Guerin, Andrea, Hashemi, Bita, Helal, Mayada, Hewson, Stacy, Inbar-Feigenberg, Michal, Kannu, Peter, Karp, Natalya, Kim, Raymond H, Kronick, Jonathan, Liston, Eriskay, MacDonald, Heather, Mercimek-Mahmutoglu, Saadet, Mendoza-Londono, Roberto, Nasr, Enas, Nimmo, Graeme, Parkinson, Nicole, Quercia, Nada, Raiman, Julian, Roifman, Maian, Schulze, Andreas, Shugar, Andrea, Shuman, Cheryl, Sinajon, Pierre, Siriwardena, Komudi, Weksberg, Rosanna, Yoon, Grace, Carew, Chris, Erickson, Raith, Leach, Richard A, Klein, Robert, Ray, Peter N, Meyn, M Stephen, Scherer, Stephen W, Cohn, Ronald D, Marshall, Christian R

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The mutational spectrum of human malignant autosomal recessive osteopetrosis by SOBACCHI, Cristina, FRATTINI, Annalisa, DUPUIS-GIROD, Sophie, ELLIS, Ian, ETZIONI, Amos, FASTH, Anders, FISHER, Alain, GERRITSEN, Bert, GULINO, Virginia, HORWITZ, Edwin, KLAMROTH, Verena, LANINO, Edoardo, ORCHARD, Paul, MIROLO, Massimiliano, MUSIO, Antonio, MATTHIJS, Gert, NONOMAYA, Shigeaki, NOTARANGELO, Luigi D, OCHS, Hans D, SUPERTI FURGA, Andrea, VALIAHO, Jouni, VAN HOVE, Johan L. K, VIHINEN, Mauno, PORRAS, Oscar, VUJIC, Dragana, VEZZONI, Paolo, VILLA, Anna, TEZCAN, Ilhan, ANDOLINA, Marino, BABUL-HIRJI, Riyana, BARIC, Ivo, CANHAM, Natalie, CHITAYAT, David

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Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study-preliminary data by Allingham-Hawkins, Diane J., Babul-Hirji, Riyana, Chitayat, David, Holden, Jeanette J.A., Yang, Kathy T., Lee, C., Hudson, R., Gorwill, H., Nolin, Sarah L., Glicksman, Anne, Jenkins, Edmund C., Brown, W. Ted, Howard-Peebles, Patricia N., Becchi, Cindy, Cummings, Emilie, Fallon, Lee, Seitz, Suzanne, Black, Susan H., Vianna-Morgante, Angela M., Costa, Silvia S., Otto, Paulo A., Mingroni-Netto, Regina C., Murray, Anna, Webb, J., MacSwinney, F., Dennis, N., Jacobs, Patricia A., Syrrou, Maria, Georgiou, Ioannis, Patsalis, Phillipos C., Giovannucci Uzielli, Maria L., Guarducci, S., Lapi, E., Cecconi, A., Ricci, U., Ricotti, G., Biondi, C., Scarselli, B., Vieri, F.

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