The trisomy 18 syndrome von Cereda, Anna, Carey, John C

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Etiology and clinical presentation of birth defects: population based study von Feldkamp, Marcia L, Carey, John C, Byrne, Janice L B, Krikov, Sergey, Botto, Lorenzo D

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Elements of morphology: General terms for congenital anomalies von Hennekam, Raoul C., Biesecker, Leslie G., Allanson, Judith E., Hall, Judith G., Opitz, John M., Temple, I Karen, Carey, John C.

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Mycophenolate mofetil embryopathy: A newly recognized teratogenic syndrome von Perez-Aytes, Antonio, Marin-Reina, Purificacion, Boso, Virginia, Ledo, Ana, Carey, John C, Vento, Maximo

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Survival Outcomes of Infants with the Trisomy 13 or Trisomy 18 Syndromes von Carey, John C.

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The pathogenesis of gastroschisis von Feldkamp, Marcia L., Carey, John C.

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Novel signal transducer and activator of transcription 3 (STAT3) mutations, reduced TH17 cell numbers, and variably defective STAT3 phosphorylation in hyper-IgE syndrome von Renner, Ellen D., Rylaarsdam, Stacey, Aňover-Sombke, Stephanie, Rack, Anita L., Reichenbach, Janine, Carey, John C., Zhu, Qili, Jansson, Annette F., Barboza, Julia, Schimke, Lena F., Leppert, Mark F., Getz, Melissa M., Seger, Reinhard A., Hill, Harry R., Belohradsky, Bernd H., Torgerson, Troy R., Ochs, Hans D.

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Development of gastroschisis: Review of hypotheses, a novel hypothesis, and implications for research von Feldkamp, Marcia L., Carey, John C., Sadler, Thomas W.

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Gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritization von Di Sera, Tonya, Velinder, Matt, Ward, Alistair, Qiao, Yi, Georges, Stephanie, Miller, Chase, Pitman, Anders, Richards, Will, Ekawade, Aditya, Viskochil, David, Carey, John C., Pace, Laura, Bale, Jim, Clardy, Stacey L., Andrews, Ashley, Botto, Lorenzo, Marth, Gabor

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Further Delineation of Deletion 1p36 Syndrome in 60 Patients: A Recognizable Phenotype and Common Cause of Developmental Delay and Mental Retardation von Battaglia, Agatino, Hoyme, H. Eugene, Dallapiccola, Bruno, Zackai, Elaine, Hudgins, Louanne, McDonald-McGinn, Donna, Bahi-Buisson, Nadia, Romano, Corrado, Williams, Charles A, Brailey, Lisa L, Zuberi, Sameer M, Carey, John C

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Emerging evidence that medical and surgical interventions improve the survival and outcome in the trisomy 13 and 18 syndromes von Carey, John C.

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Mutations in embryonic myosin heavy chain ( MYH3 ) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome von Bamshad, Michael J, Toydemir, Reha M, Rutherford, Ann, Whitby, Frank G, Jorde, Lynn B, Carey, John C

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Author Correction: Gene.iobio: an interactive web tool for versatile, clinically-driven variant interrogation and prioritization von Di Sera, Tonya, Velinder, Matt, Ward, Alistair, Qiao, Yi, Georges, Stephanie, Miller, Chase, Pitman, Anders, Richards, Will, Ekawade, Aditya, Viskochil, David, Carey, John C., Pace, Laura, Bale, Jim, Clardy, Stacey L., Andrews, Ashley, Botto, Lorenzo, Marth, Gabor

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Parent‐authored memoirs: Lessons in the practice of narrative medicine von Carey, John C.

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Fine-grained facial phenotype-genotype analysis in Wolf-Hirschhorn syndrome von Hammond, Peter, Hannes, Femke, Suttie, Michael, Devriendt, Koen, Vermeesch, Joris Robert, Faravelli, Francesca, Forzano, Francesca, Parekh, Susan, Williams, Steve, McMullan, Dominic, South, Sarah T, Carey, John C, Quarrell, Oliver

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Perspectives on the care and management of infants with trisomy 18 and trisomy 13: striving for balance von Carey, John C

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Double Inactivation of NF1 in Tibial Pseudarthrosis von Stevenson, David A., Zhou, Holly, Ashrafi, Shadi, Messiaen, Ludwine M., Carey, John C., D’Astous, Jacques L., Santora, Stephen D., Viskochil, David H.

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The Splicing Efficiency of Activating HRAS Mutations Can Determine Costello Syndrome Phenotype and Frequency in Cancer von Hartung, Anne-Mette, Swensen, Jeff, Uriz, Inaki E, Lapin, Morten, Kristjansdottir, Karen, Petersen, Ulrika S S, Bang, Jeanne Mari V, Guerra, Barbara, Andersen, Henriette Skovgaard, Dobrowolski, Steven F, Carey, John C, Yu, Ping, Vaughn, Cecily, Calhoun, Amy, Larsen, Martin R, Dyrskjøt, Lars, Stevenson, David A, Andresen, Brage S

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A Novel Mutation in FGFR3 Causes Camptodactyly, Tall Stature, and Hearing Loss (CATSHL) Syndrome von Toydemir, Reha M., Brassington, Anna E., Bayrak-Toydemir, Pınar, Krakowiak, Patrycja A., Jorde, Lynn B., Whitby, Frank G., Longo, Nicola, Viskochil, David H., Carey, John C., Bamshad, Michael J.

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Elements of morphology: Introduction von Allanson, Judith E., Biesecker, Leslie G., Carey, John C., Hennekam, Raoul C.M.

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