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Showing results 1 to 2 of 2
Title
Author(s)
Issue Date
Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion
Journal:
American Journal of Medical Genetics, Part A
Aldinger, KA
Kogan, J
Kimonis, V
Fernandez, B
Horn, D
Klopocki, E
Chung, B
Toutain, A
Weksberg, R
Millen, KJ
Barkovich, AJ
Dobyns, WB
2013
Phenotypic spectrum associated with PTCHD1 deletion and truncating mutations includes intellectual disability and autism spectrum disorder
Journal:
Clinical Genetics
Chaudhry, A
Noor, A
Degagne, B
Baker, K
Bok, LA
Brady, AF
Chitayat, D
Chung, BHY
Cytrynbaum, C
Dyment, D
Filges, I
Helm, B
Hutchison, HT
Jeng, LJB
Laumonnier, F
Marshall, CR
Menzel, M
Parkash, S
Parker, MJ
The, DDD STUDY
Raymond, FL
Rideout, AL
Roberts, W
Rupps, R
Schanze, I
Schrander-Stumpel, CTRM
Speevak, MD
Stavropoulos, DJ
Stevens, SJC
Thomas, ERA
Toutain, A
Vergano, S
Weksberg, R
Scherer, SW
Vincent, JB
Carter, MT
2015