The Disabled Young Adult: Ready to Leave Home?

Por Tervo, Raymond, O'Leary, Donal
Publicado em 1986

The Child with Delayed Language: Assessment and Management

Por Tervo, Raymond C., Kinney, Cheryl A.
Publicado em 1981

22q13.32 Deletion and Duplication and Inversion in the Same Family: A Rare Occurrence

Por Jafri, Farooqua, Fink, James, Higgins, Rodney R., Tervo, Raymond
Publicado em 2011

Parent Reported Pain in Rett Syndrome

Por Symons, Frank J., Byiers, Breanne, Tervo, Raymond, Beisang, Arthur
Publicado em 2013

Seizures and Pain Uncertainty Associated with Parenting Stress and Rett Syndrome

Por Byiers, Breanne J., Tervo, Raymond C., Feyma, Timothy J., Symons, Frank J.
Publicado em 2013

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
Publicado no Dev Med Child Neurol (2014)

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.
Publicado no Dev Psychopathol (2018)

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.
Publicado no J Pediatr Psychol (2016)

Peripheral Innervation in Children with Global Developmental Delay: Biomarker for Risk for Self-Injurious Behavior?

Por Symons, Frank J., Tervo, Raymond C., Barney, Chantel C., Damerow, John, Selim, Mona, McAdams, Brian, Foster, Shawn, Crabb, Gwen Wendelschafer, Kennedy, William
Publicado no J Child Neurol (2015)

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
Publicado em 2008

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
Publicado no Am J Med Genet A (2013)

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.
Publicado em 2014