The Glanders Organism with Reference to Its Cell Inclusions

Por Worley, Gordon, Young, Gerald
Publicado em 1945

Bacteriophagy of Bacillus mycoides with Reference to Effect on Dissociation and Transmission by Spores

Por Lewis, I. M., Worley, Gordon
Publicado em 1936

The Comparative Pathology of Rhabdomyosarcoma with a Report of a Case in a Dog

Por Worley, Gordon, Gorham, John R.
Publicado em 1954

Frequency of Celiac Disease in Individuals with Down Syndrome in the United States

Por Mackey, Joanne, Treem, William R., Worley, Gordon, Boney, Anne, Hart, Patricia, Kishnani, Priya S.
Publicado em 2001

New Onset Focal Weakness in Children With Down Syndrome

Por Worley, Gordon, Shbarou, Rolla, Heffner, Amy N., Belsito, Karin M., Capone, George T., Kishnani, Priya S.
Publicado em 2004

Hypothyroidism in Down Syndrome: Screening Guidelines and Testing Methodology

Por Hardy, Olga, Worley, Gordon, Lee, Mary M., Chaing, Shu, Mackey, Joanne, Crissman, Blythe, Kishnani, Priya Sunil
Publicado em 2004

Prevalence of Iron Deficiency in Children with Down Syndrome

Por Dixon, Natalia E, Crissman, Blythe G, Smith, P Brian, Zimmerman, Sherri A, Worley, Gordon, Kishnani, Priya S
Publicado em 2010

Apolipoprotein E ɛ4 Allele and Outcomes of Traumatic Spinal Cord Injury

Por Jha, Amitabh, Lammertse, Daniel P, Coll, Joseph R, Charlifue, Susan, Coughlin, Christopher T, Whiteneck, Gale G, Worley, Gordon
Publicado em 2008

Magnetic Susceptibility of Brain Iron is Associated with Childhood Spatial IQ

Por Carpenter, Kimberly L.H., Li, Wei, Wei, Hongjiang, Wu, Bing, Xiao, Xue, Liu, Chunlei, Worley, Gordon, Egger, Helen Link
Publicado no Neuroimage (2016)

Diffuse reduction of white matter connectivity in cerebral palsy with specific vulnerability of long range fiber tracts()

Por Englander, Zoë A., Pizoli, Carolyn E., Batrachenko, Anastasiya, Sun, Jessica, Worley, Gordon, Mikati, Mohamad A., Kurtzberg, Joanne, Song, Allen W.
Publicado em 2013

The accuracy of photoscreening at detecting treatable ocular conditions in children with Down syndrome

Por Yanovitch, Tammy, Wallace, David K., Freedman, Sharon F., Enyedi, Laura B., Kishnani, Priya, Worley, Gordon, Crissman, Blythe, Burner, Erica, Young, Terri L.
Publicado em 2010

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

Por Worley Gordon, Langford Cordelia F, Ellis Peter, Wright Harry H, Abramson Ruth K, Lintas Carla, Markunas Christina A, Biscocho Dhani, Johnson Jessica, Towers Aaron J, Connelly Jessica J, Gregory Simon G, Delong G Robert, Murphy Susan K, Cuccaro Michael L, Persico Antonello, Pericak-Vance Margaret A
Publicado em 2009-10-01

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

Por Gregory, Simon G, Connelly, Jessica J, Towers, Aaron J, Johnson, Jessica, Biscocho, Dhani, Markunas, Christina A, Lintas, Carla, Abramson, Ruth K, Wright, Harry H, Ellis, Peter, Langford, Cordelia F, Worley, Gordon, Delong, G Robert, Murphy, Susan K, Cuccaro, Michael L, Persico, Antonello, Pericak-Vance, Margaret A
Publicado em 2009

Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios

Por Zhu, Xiaolin, Petrovski, Slavé, Xie, Pingxing, Ruzzo, Elizabeth K., Lu, Yi-Fan, McSweeney, K. Melodi, Ben-Zeev, Bruria, Nissenkorn, Andreea, Anikster, Yair, Oz-Levi, Danit, Dhindsa, Ryan S., Hitomi, Yuki, Schoch, Kelly, Spillmann, Rebecca C., Heimer, Gali, Marek-Yagel, Dina, Tzadok, Michal, Han, Yujun, Worley, Gordon, Goldstein, Jennifer, Jiang, Yong-Hui, Lancet, Doron, Pras, Elon, Shashi, Vandana, McHale, Duncan, Need, Anna C., Goldstein, David B.
Publicado no Genet Med (2015)