Hakutulokset - Tervo, Raymond

The Disabled Young Adult: Ready to Leave Home? Tekijä Tervo, Raymond, O'Leary, Donal

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The Child with Delayed Language: Assessment and Management Tekijä Tervo, Raymond C., Kinney, Cheryl A.

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22q13.32 Deletion and Duplication and Inversion in the Same Family: A Rare Occurrence Tekijä Jafri, Farooqua, Fink, James, Higgins, Rodney R., Tervo, Raymond

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Parent Reported Pain in Rett Syndrome Tekijä Symons, Frank J., Byiers, Breanne, Tervo, Raymond, Beisang, Arthur

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Seizures and Pain Uncertainty Associated with Parenting Stress and Rett Syndrome Tekijä Byiers, Breanne J., Tervo, Raymond C., Feyma, Timothy J., Symons, Frank J.

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Skin and self-injury: a possible link between peripheral innervation and immune function? Tekijä Symons, Frank J, Gilles, Elizabeth, Tervo, Raymond, Wendelschafer-Crabb, Gwen, Panoutsopoulou, Ioanna, Kennedy, William

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Proopiomelanocortin (POMC) sequencing and developmental delay: Preliminary evidence for a SNP in the 3’ UTR region of the POMC gene—Possible relevance for biological risk and self-... Tekijä DAMEROW, JOHN A., TERVO, RAYMOND C., EHRHARDT, MICHAEL, PANOSKALTSIS-MORTARI, ANGELA, SYMONS, FRANK J.

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Comparative Analysis of Self-Injurious Behaviour Topographies in Young Children with and without Developmental Delay Tekijä MacLean, William E., Damian, Adele F., Hoch, John, Tervo, Raymond T., Symons, Frank J.

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A Direct Comparison of Self-Injurious and Stereotyped Motor Behavior Between Preschool-Aged Children With and Without Developmental Delays Tekijä Hoch, John, Spofford, Lisa, Dimian, Adele, Tervo, Raymond, MacLean, William E., Symons, Frank J.

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Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication Tekijä Ballif, Blake C, Theisen, Aaron, Coppinger, Justine, Gowans, Gordon C, Hersh, Joseph H, Madan-Khetarpal, Suneeta, Schmidt, Karen R, Tervo, Raymond, Escobar, Luis F, Friedrich, Christopher A, McDonald, Marie, Campbell, Lindsey, Ming, Jeffrey E, Zackai, Elaine H, Bejjani, Bassem A, Shaffer, Lisa G

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The duplication 17p13.3 phenotype: Analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes Tekijä Curry, Cynthia J, Rosenfeld, Jill A, Grant, Erica, Gripp, Karen W, Anderson, Carol, Aylsworth, Arthur S, Ben Saad, Taha, Chizhikov, Victor V, Dybose, Giedre, Fagerberg, Christina, Falco, Michelle, Fels, Christina, Fichera, Marco, Graakjaer, Jesper, Greco, Donatella, Hair, Jennifer, Hopkins, Elizabeth, Huggins, Marlene, Ladda, Roger, Li, Chumei, Moeschler, John, Nowaczyk, Malgorzata JM, Ozmore, Jillian R, Reitano, Santina, Romano, Corrado, Roos, Laura, Schnur, Rhonda E, Sell, Susan, Suwannarat, Pim, Svaneby, Dea, Szybowska, Marta, Tarnopolsky, Mark, Tervo, Raymond, Tsai, Anne Chun-Hui, Tucker, Megan, Vallee, Stephanie, Wheeler, Ferrin C, Zand, Dina J, Barkovich, A James, Aradhya, Swaroop, Shaffer, Lisa G, Dobyns, William B

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Refining analyses of copy number variation identifies specific genes associated with developmental delay Tekijä Coe, Bradley P., Witherspoon, Kali, Rosenfeld, Jill A., van Bon, Bregje W.M., Vulto-van Silfhout, Anneke T., Bosco, Paolo, Friend, Kathryn L., Baker, Carl, Buono, Serafino, Vissers, Lisenka E.L.M., Schuurs-Hoeijmakers, Janneke H., Hoischen, Alex, Pfundt, Rolph, Krumm, Nik, Carvill, Gemma L., Li, Deana, Amaral, David, Brown, Natasha, Lockhart, Paul J., Scheffer, Ingrid E, Alberti, Antonino, Shaw, Marie, Pettinato, Rosa, Tervo, Raymond, de Leeuw, Nicole, Reijnders, Margot R.F., Torchia, Beth S., Peeters, Hilde, O'Roak, Brian J., Fichera, Marco, Hehir-Kwa, Jayne Y., Shendure, Jay, Mefford, Heather C., Haan, Eric, Gécz, Jozef, de Vries, Bert B.A., Romano, Corrado, Eichler, Evan E.

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