Suchergebnisse - Tervo, Raymond

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

Volltext Volltext

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

Volltext Volltext

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

Volltext Volltext Volltext

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

Volltext Volltext Volltext

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

Volltext Volltext Volltext

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

Volltext Volltext Volltext

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-... von DAMEROW, JOHN A., TERVO, RAYMOND C., EHRHARDT, MICHAEL, PANOSKALTSIS-MORTARI, ANGELA, SYMONS, FRANK J.

Volltext Volltext Volltext

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

Volltext Volltext Volltext

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

Volltext Volltext Volltext

Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication von 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

Volltext Volltext Volltext

The duplication 17p13.3 phenotype: Analysis of 21 families delineates developmental, behavioral and brain abnormalities, and rare variant phenotypes von 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

Volltext Volltext Volltext

Refining analyses of copy number variation identifies specific genes associated with developmental delay von 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.

Volltext Volltext Volltext