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    Delivery Room Resuscitation and Short-Term Outcomes in Moderately Preterm Infants von Natarajan, Girija, Shankaran, Seetha, Wyckoff, Myra, Laptook, Abbot R., Bell, Edward F., Carlo, Waldemar A., Saha, Shampa, Van Meurs, Krisa P., Sanchez, Pablo J., D'Angio, Carl T., Higgins, Rosemary D., Newman, Nancy, Walsh, Michele C., Polin, Richard A., Hensman, Angelita M., Vieira, Elisa, Siner, Bonnie S., Pallotto, Eugenia K., Kilbride, Howard W., Gauldin, Cheri, Holmes, Anne, Johnson, Kathy, Poindexter, Brenda B., Schibler, Kurt, Kallapur, Suhas G., Grisby, Cathy, Alexander, Barbara, Fischer, Estelle E., Jackson, Lenora, Kirker, Kristin, Jennings, Jennifer, Wuertz, Sandra, Muthig, Greg, Goldberg, Ronald N., Finkle, Joanne, Fisher, Kimberley A., Bernhardt, Janice, Clark, Cindy, Carlton, David P., Bottcher, Diane I., Archer, Stephanie Wilson, Sokol, Greg, Herron, Dianne E., Nelin, Leif D., Luzader, Patricia, Parikh, Nehal A., Nist, Marliese Dion, Fuller, Jennifer, McGregor, Sarah, Rodgers, Elizabeth, Ulloa, Jodi A., Wolfe, Tara, Wallace, Dennis, Crawford, Margaret, Gabrio, Jenna, Kandefer, Sarah, O'Donnell Auman, Jeanette, Stevenson, David K., Ambalavanan, Namasivayam, Collins, Monica V., Cosby, Shirley S., Devaskar, Uday, Geller, Rachel, Colaizy, Tarah T., Ellsbury, Dan L., Brumbaugh, Jane E., Johnson, Karen J., Campbell, Donia B., Walker, Jacky R., Watterberg, Kristi L., Lacy, Conra Backstrom, Beauman, Sandy Sundquist, Hartenberger, Carol, Kirpalani, Haresh, DeMauro, Sara B., Cook, Noah, Chaudhary, Aasma S., Cucinotta, Dara, Lakshminrusimha, Satyan, Scorsone, Ann Marie, Hunn, Julianne, Jensen, Rosemary, Wadkins, Holly I.M., Guilford, Stephanie, Brion, Luc P., Vasil, Diana M., Chen, Lijun, Torres, Lizette E., Kennedy, Kathleen A., Tyson, Jon E., Arldt-McAlister, Julie, Garcia, Carmen, Martin, Karen, McDavid, Georgia E., Wright, Sharon L., Pappas, Athina, Barks, John, Handel, Shelley, White, Diane F., Christensen, Mary

    Veröffentlicht in The Journal of pediatrics

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    Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities von Cali, Elisa, Suri, Mohnish, Scala, Marcello, Ferla, Matteo P., Alavi, Shahryar, Faqeih, Eissa Ali, Bijlsma, Emilia K., Wigby, Kristen M., Baralle, Diana, Mehrjardi, Mohammad Y.V., Schwab, Jennifer, Platzer, Konrad, Steindl, Katharina, Hashem, Mais, Jones, Marilyn, Niyazov, Dmitriy M., Jacober, Jennifer, Littlejohn, Rebecca Okashah, Weis, Denisa, Zadeh, Neda, Rodan, Lance, Goldenberg, Alice, Lecoquierre, François, Dutra-Clarke, Marina, Horvath, Gabriella, Young, Dana, Orenstein, Naama, Bawazeer, Shahad, Vulto-van Silfhout, Anneke T., Herenger, Yvan, Dehghani, Mohammadreza, Seyedhassani, Seyed Mohammad, Bahreini, Amir, Nasab, Mahya E., Ercan-Sencicek, A. Gulhan, Firoozfar, Zahra, Movahedinia, Mojtaba, Efthymiou, Stephanie, Striano, Pasquale, Karimiani, Ehsan Ghayoor, Salpietro, Vincenzo, Taylor, Jenny C., Redman, Melody, Stegmann, Alexander P.A., Laner, Andreas, Abdel-Salam, Ghada, Li, Megan, Bengala, Mario, Müller, Amelie Johanna, Digilio, Maria C., Rauch, Anita, Gunel, Murat, Titheradge, Hannah, Schweitzer, Daniela N., Kraus, Alison, Valenzuela, Irene, McLean, Scott D., Phornphutkul, Chanika, Salih, Mustafa, Begtrup, Amber, Schnur, Rhonda E., Torti, Erin, Haack, Tobias B., Prada, Carlos E., Alkuraya, Fowzan S., Houlden, Henry, Maroofian, Reza

    Veröffentlicht in Genetics in medicine

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