KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis von Gueneau, Lucie, Fish, Richard J., Shamseldin, Hanan E., Voisin, Norine, Tran Mau-Them, Frédéric, Preiksaitiene, Egle, Monroe, Glen R., Lai, Angeline, Putoux, Audrey, Allias, Fabienne, Ambusaidi, Qamariya, Ambrozaityte, Laima, Cimbalistienė, Loreta, Delafontaine, Julien, Guex, Nicolas, Hashem, Mais, Kurdi, Wesam, Jamuar, Saumya Shekhar, Ying, Lim J., Bonnard, Carine, Pippucci, Tommaso, Pradervand, Sylvain, Roechert, Bernd, van Hasselt, Peter M., Wiederkehr, Michaël, Wright, Caroline F., Xenarios, Ioannis, van Haaften, Gijs, Shaw-Smith, Charles, Schindewolf, Erica M., Neerman-Arbez, Marguerite, Sanlaville, Damien, Lesca, Gaëtan, Guibaud, Laurent, Reversade, Bruno, Chelly, Jamel, Kučinskas, Vaidutis, Alkuraya, Fowzan S., Reymond, Alexandre

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Enlarged cavum septum pellucidum and small thymus as markers for 22q11.2 deletion syndrome von Gaiser, Kimberly B., Schindewolf, Erica M., Conway, Laura J., Coleman, Beverly G., Oliver, Edward R., Rychik, Jack R., Debari, Suzanne E., Mcdonald‐Mcginn, Donna M., Zackai, Elaine H., Moldenhauer, Julie S., Gebb, Juliana S.

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Prenatal cerebral imaging features of a new syndromic entity related to KIAA1109 pathogenic variants mimicking tubulinopathy von Cabet, Sara, Putoux, Audrey, Buenerd, Annie, Gueneau, Lucie, Reymond, Alexandre, Thia, Edwin W.H., Lai, Angeline H.M., Schindewolf, Erica M., Sanlaville, Damien, Lesca, Gaetan, Guibaud, Laurent

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Autism spectrum disorder and neurodevelopmental delays in children with giant omphalocele von Danzer, Enrico, Hoffman, Casey, Miller, Judith S., D'Agostino, Jo Ann, Schindewolf, Erica M., Gerdes, Marsha, Bernbaum, Judy, Adams, Samantha E., Rintoul, Natalie E., Herkert, Lisa M., Taylor, Lynne, Schreiber, Jane, Peranteau, William H., Flake, Alan W., Adzick, N. Scott, Hedrick, Holly L.

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93 Reliability of “lethal” ultrasound markers in identifying fetuses with truly life-limiting skeletal dysplasia von Crane, Haley, Schindewolf, Erica M., Moldenhauer, Julie, Burrill, Natalie, DeBari, Suzanne, Khalek, Nahla, Teefey, Christina Paidas, Soni, Shelly, Coleman, Beverly G., Gebb, Juliana S.

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177 Value of “lethal” ultrasound markers identifying fetuses with lethal skeletal dysplasia before/after 28 weeks von Crane, Haley, Schindewolf, Erica M., Moldenhauer, Julie, Burrill, Natalie, DeBari, Suzanne, Khalek, Nahla, Teefey, Christina Paidas, Soni, Shelly, Coleman, Beverly G., Gebb, Juliana S.

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743 Utility of genetic testing in fetuses with suspected lethal skeletal dysplasia on sonography von Crane, Haley, Schindewolf, Erica M., Gebb, Juliana S., Burrill, Natalie, Pilchman, Lisa, Wright, Renee, DeBari, Suzanne, Coleman, Beverly G., Moldenhauer, Julie

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Perinatal depressive risk in pregnancies complicated by fetal anomalies von Moldenhauer, Julie S., Teefey, Christina Paidas, Budney, Alexandria, Soni, Shelly, Gebb, Juliana S., Khalek, Nahla, Schindewolf, Erica M., Cole, Joanna

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Whole Exome Sequencing in an Enriched Population of Fetuses with Structural Anomalies von Burrill, Natalie, Schindewolf, Erica M., Pilchman, Lisa, Dicicco, Renee, Khalek, Nahla, Gebb, Juliana S., Teefey, Christina Paidas, Soni, Shelly, Oliver, Edward R., Linn, Rebecca, Moldenhauer, Julie S.

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Enlarged cavum septum pellucidum and small thymus as markers for 22q11.2 deletion syndrome von Gaiser, Kimberly B., Schindewolf, Erica M., Moldenhauer, Julie S., Coleman, Beverly G., Oliver, Edward R., Rychik, Jack R., McDonald-McGinn, Donna, Gebb, Juliana S.

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What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia von Campbell, Ian M., Sheppard, Sarah E., Crowley, T. Blaine, McGinn, Daniel E., Bailey, Alice, McGinn, Michael J., Unolt, Marta, Homans, Jelle F., Chen, Erin Y., Salmons, Harold I., Gaynor, J. William, Goldmuntz, Elizabeth, Jackson, Oksana A., Katz, Lorraine E., Mascarenhas, Maria R., Deeney, Vincent F. X., Castelein, René M., Zur, Karen B., Elden, Lisa, Kallish, Staci, Kolon, Thomas F., Hopkins, Sarah E., Chadehumbe, Madeline A., Lambert, Michele P., Forbes, Brian J., Moldenhauer, Julie S., Schindewolf, Erica M., Solot, Cynthia B., Moss, Edward M., Gur, Raquel E., Sullivan, Kathleen E., Emanuel, Beverly S., Zackai, Elaine H., McDonald‐McGinn, Donna M.

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"Who is the deciding factor?" Analysis of parental perspectives regarding discontinuation of elaprase in children with MPS II von Schindewolf, Erica M., Conway, Laura J., Chadwick, Sara L.

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KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis von Gueneau, Lucie, Fish, Richard J, Shamseldin, Hanan E, Voisin, Norine, Tran Mau-Them, Frédéric, Preiksaitiene, Egle, Monroe, Glen R, Lai, Angeline, Putoux, Audrey, Allias, Fabienne, Ambusaidi, Qamariya, Ambrozaityte, Laima, Cimbalistienė, Loreta, Delafontaine, Julien, Guex, Nicolas, Hashem, Mais, Kurdi, Wesam, Jamuar, Saumya Shekhar, Ying, Lim J, Bonnard, Carine, Pippucci, Tommaso, Pradervand, Sylvain, Roechert, Bernd, van Hasselt, Peter M, Wiederkehr, Michaël, Wright, Caroline F, Xenarios, Ioannis, van Haaften, Gijs, Shaw-Smith, Charles, Schindewolf, Erica M, Neerman-Arbez, Marguerite, Sanlaville, Damien, Lesca, Gaëtan, Guibaud, Laurent, Reversade, Bruno, Chelly, Jamel, Kučinskas, Vaidutis, Alkuraya, Fowzan S, Reymond, Alexandre, DDD Study

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What’s New with 22q? An update from the 22q and You Center at the Children’s Hospital of Philadelphia von Campbell, Ian M., Sheppard, Sarah E., Crowley, T. Blaine, McGinn, Daniel E., Bailey, Alice, McGinn, Michael J., Unolt, Marta, Homans, Jelle F., Chen, Erin Y., Salmons, Harold I., Gaynor, J. William, Goldmuntz, Elizabeth, Jackson, Oksana A., Katz, Lorraine E., Mascarenhas, Maria R., Deeney, Vincent F. X., Castelein, Rene M., Zu, Karen B., Elden, Lisa, Kallish, Staci, Kolon, Thomas F., Hopkins, Sarah E., Chadehumbe, Madeline A., Lambert, Michele P., Forbes, Brian J., Moldenhauer, Julie S., Schindewolf, Erica M., Solot, Cynthia B., Moss, Edward M., Gur, Raquel E., Sullivan, Kathleen E., Emanuel, Beverly S., Zackai, Elaine H., McDonald-McGinn, Donna M.

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Cover Image, Volume 176A, Number 10, October 2018 von Campbell, Ian M., Sheppard, Sarah E., Crowley, T. Blaine, McGinn, Daniel E., Bailey, Alice, McGinn, Michael J., Unolt, Marta, Homans, Jelle F., Chen, Erin Y., Salmons, Harold I., Gaynor, J. William, Goldmuntz, Elizabeth, Jackson, Oksana A., Katz, Lorraine E., Mascarenhas, Maria R., Deeney, Vincent F. X., Castelein, René M., Zur, Karen B., Elden, Lisa, Kallish, Staci, Kolon, Thomas F., Hopkins, Sarah E., Chadehumbe, Madeline A., Lambert, Michele P., Forbes, Brian J., Moldenhauer, Julie S., Schindewolf, Erica M., Solot, Cynthia B., Moss, Edward M., Gur, Raquel E., Sullivan, Kathleen E., Emanuel, Beverly S., Zackai, Elaine H., McDonald‐McGinn, Donna M.

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Implementation of Trauma-Informed Care Strategies in a Multidisciplinary Maternal-Fetal Care Center [A186] von Cole, Joanna CM, Zajac, Lindsay, Budney, Alexandra, Spinner, Susan, Schindewolf, Erica, Teefey, Christina Paidas

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Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome von Óskarsdóttir, Sólveig, Boot, Erik, Crowley, Terrence Blaine, Loo, Joanne C.Y., Arganbright, Jill M., Armando, Marco, Baylis, Adriane L., Breetvelt, Elemi J., Castelein, René M., Chadehumbe, Madeline, Cielo, Christopher M., de Reuver, Steven, Eliez, Stephan, Fiksinski, Ania M., Forbes, Brian J., Gallagher, Emily, Hopkins, Sarah E., Jackson, Oksana A., Levitz-Katz, Lorraine, Klingberg, Gunilla, Lambert, Michele P., Marino, Bruno, Mascarenhas, Maria R., Moldenhauer, Julie, Moss, Edward M., Nowakowska, Beata Anna, Orchanian-Cheff, Ani, Putotto, Carolina, Repetto, Gabriela M., Schindewolf, Erica, Schneider, Maude, Solot, Cynthia B., Sullivan, Kathleen E., Swillen, Ann, Unolt, Marta, Van Batavia, Jason P., Vingerhoets, Claudia, Vorstman, Jacob, Bassett, Anne S., McDonald-McGinn, Donna M.

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Loss‐of‐function of Endothelin receptor type A results in Oro‐Oto‐Cardiac syndrome von Pritchard, Amanda Barone, Kanai, Stanley M., Krock, Bryan, Schindewolf, Erica, Oliver‐Krasinski, Jennifer, Khalek, Nahla, Okashah, Najeah, Lambert, Nevin A., Tavares, Andre L.P., Zackai, Elaine, Clouthier, David E.

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The Reliability of Ultrasound Markers in Identifying Fetuses With a Life‐Limiting Skeletal Dysplasia von Crane, Haley M., Schindewolf, Erica, Burrill, Natalie, Debari, Suzanne, Khalek, Nahla, Paidas Teefey, Christina, Soni, Shelly, Coleman, Beverly, Moldenhauer, Julie S., Gebb, Juliana

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Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions von Blagowidow, Natalie, Nowakowska, Beata, Schindewolf, Erica, Grati, Francesca Romana, Putotto, Carolina, Breckpot, Jeroen, Swillen, Ann, Crowley, Terrence Blaine, Loo, Joanne C Y, Lairson, Lauren A, Óskarsdóttir, Sólveig, Boot, Erik, Garcia-Minaur, Sixto, Cristina Digilio, Maria, Marino, Bruno, Coleman, Beverly, Moldenhauer, Julie S, Bassett, Anne S, McDonald-McGinn, Donna M

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