Resultados de búsqueda - Tervo, Raymond

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

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

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

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

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Seizures and Pain Uncertainty Associated with Parenting Stress and Rett Syndrome por 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? por 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-... por 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 por 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 por 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 por 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 por 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 por 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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