Outcomes of Teacher Professional Development and Learning in Addressing Challenging Behaivour in Vietnamese Students with Intellectual Disability: A Pilot Study

- Pham, Thi Quynh Ni, Arthur-Kelly, Michael, Foggett, Judith, Lyons, Gordon

De novo variants in CNOT1, a central component of the CCR4-NOT complex involved in gene expression and RNA and protein stability, cause neurodevelopmental delay

- Vissers, Lisenka E. L. M., Kalvakuri, Sreehari, de Boer, Elke, Geuer, Sinje, Oud, Machteld, van Outersterp, Inge, Kwint, Michael, Witmond, Melde, Kersten, Simone, Polla, Daniel L., Weijers, Dilys, Begtrup, Amber, McWalter, Kristy, Ruiz, Anna, Gabau, Elisabeth, Morton, Jenny E. V., Griffith, Christopher, Weiss, Karin, Gamble, Candace, Bartley, James, Goel, Himanshu

Travelling with two: balancing identity and risk in mothers with intellectual disability

- Williams, Namira Edwina

Expansion of phenotype of DDX3X syndrome: six new cases

- Beal, Bryony, Hayes, Ian, Mcgaughran, Julie, Amor, David J., Miteff, Christina, Jackson, Victoria, van Reyk, Olivia, Subramanian, Gopinath, Hildebrand, Michael S., Morgan, Angela T., Goel, Himanshu

Teacher professional development and learning to support students with intellectual disability and challenging behaviour: a study in special education settings in Vietnam

- Pham, Thi Quynh Ni

Teachers attitudes towards use of information communication technology with students with intellectual disability in Saudi Arabian schools

- Alsawalem, Ibraheem Mohammed N.

Disability and madness in colonial asylum records in Australia and New Zealand

- Coleborne, Catharine

Computer face-matching technology using two-dimensional photographs accurately matches the facial gestalt of unrelated individuals with the same syndromic form of intellectual disability

- Dudding-Byth, Tracy, Baxter, Anne, Kleefstra, Tjitske, Ratwatte, Seshika, Riveros, Carlos, Brain, Steve, Lovell, Brian C., Holliday, Elizabeth G., Hackett, Anna, O'Donnell, Sheridan, White, Susan M., Attia, John, Brunner, Han, de Vries, Bert, Koolen, David

Could I, should I? Parenting aspirations and personal considerations of five young women with 22q11.2 deletion syndrome

- Phillips, Lisa, Goodwin, Jane, Johnson, Martin P., Campbell, Linda E.

Validation of the choking risk assessment and pneumonia risk assessment for adults with Intellectual and Developmental Disability (IDD)

- Sheppard, Justine Joan, Malandraki, Georgia A., Pifer, Paula, Cuff, Jill, Troche, Michelle, Hemsley, Bronwyn, Balandin, Susan, Mishra, Avinash, Hochman, Roberta

Occupational engagement and adults with intellectual disabilities

- Mahoney, Wanda J., Roberts, Elysa, Bryze, Kimberly, Kent, Judith A. Parker

Validating Kohler's Taxonomy of Transition Programming for adolescents with intellectual disability in the Chinese context

- Xu, Tianxi, Dempsey, Ian, Foreman, Phil

Social cognition dysfunction in adolescents with 22q11.2 deletion syndrome (velo-cardio-facial syndrome): relationship with executive functioning and social competence/functioning

- Campbell, L. E., McCabe, K. L., Melville, J. L., Strutt, P. A., Schall, U.

Depression and anxiety symptoms during the transition to early adulthood for people with intellectual disabilities

- Austin, Kristie

Views of Chinese parents and transition teachers on school-to-work transition services for adolescents with intellectual disability: a qualitative study

- Xu, Tianxi, Dempsey, Ian, Foreman, Phil

Engagement in retirement: an evaluation of the effect of Active Mentoring on engagement of older adults with intellectual disability in mainstream community groups

- Chng, J. P. L., Stancliffe, R. J., Wilson, N. J., Anderson, K.

FOXP1 mutations cause intellectual disability and a recognizable phenotype

- Le Fevre, Anna K., Taylor, Sharelle, Bain, Nicole, Fagan, Kerry, Hunter, Matthew F., Malek, Neva H., Horn, Denise, Carr, Christopher W., Abdul-Rahman, Omar A., O'Donnell, Sherindan, Burgess, Trent, Shaw, Marie, Gecz, Jozef

Relationships, sexuality and parenting: the experience of five young women with 22q11.2 deletion syndrome (22q11DS): an interpretative phenomenological study

- Phillips, Lisa

How much does intellectual disability really cost? First estimates for Australia

- Doran, Christopher M., Einfeld, Stewart L., Madden, Rosamond H., Otim, Michael, Horstead, Siân K., Ellis, Louise A., Emerson, Eric

CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes

- Hackett, Anna, Tarpey, Patrick S., Tolmie, John, Yates, John R. W., Turner, Gillian, WIlson, Meredith, Futreal, Andrew P., Corbett, Mark, Shaw, Marie, Gecz, Jozef, Raymond, F. Lucy, Stratton, Micahel R., Licata, Andrea, Schwartz, Charles E., Abidi, Fatima E., Cox, James, Whibley, Annabel, Boyle, Jackie, Rogers, Carolyn, Grigg, John, Partington, Michael, Stevenson, Roger E.