4
results
for author:"Szatmari P."
in Literature Citations
| Copy number variation analysis and sequencing of the X-linked mental retardation gene TSPAN7/TM4SF2 in patients with autism spectrum disorder. Noor A., Gianakopoulos P.J., Fernandez B., Marshall C.R., Szatmari P., Roberts W., Scherer S.W., Vincent J.B. Psychiatr. Genet. 19:154-155(2009) · Mapped (10) |
| Contribution of SHANK3 mutations to autism spectrum disorder. Moessner R., Marshall C.R., Sutcliffe J.S., Skaug J., Pinto D., Vincent J., Zwaigenbaum L., Fernandez B., Roberts W., Szatmari P. et al. Am. J. Hum. Genet. 81:1289-1297(2007) · Mapped (4) |
| Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia. Feuk L., Kalervo A., Lipsanen-Nyman M., Skaug J., Nakabayashi K., Finucane B., Hartung D., Innes M., Kerem B., Nowaczyk M.J. et al. Am. J. Hum. Genet. 79:965-972(2006) · Mapped (12) |
| Human chromosome 7: DNA sequence and biology. Scherer S.W., Cheung J., MacDonald J.R., Osborne L.R., Nakabayashi K., Herbrick J.-A., Carson A.R., Parker-Katiraee L., Skaug J., Khaja R. et al. Science 300:767-772(2003) · UniProtKB (658) |
