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American Journal of Human Genetics|March 20, 2001
Disruption of a novel gene (IMMP2L) by a breakpoint in 7q31 associated with Tourette syndromeE Petek, C Windpassinger, J B Vincent, et al.
Plos One|September 27, 2019
Association between distress and knowledge among parents of autistic childrenAfiqah Yusuf, Iskra Peltekova, Tal Savion-Lemieux, et al.
Research in Developmental Disabilities|March 3, 2020
Perceived utility of biological testing for autism spectrum disorder is associated with child and family functioningAfiqah Yusuf, Iskra Peltekova, Tal Savion-Lemieux, et al.
Insects|September 1, 2017
Efficacy of Chlorantraniliprole in Controlling Structural Infestations of the Eastern Subterranean Termite in the USASusan C Jones, Edward L Vargo, T Chris Keefer, et al.
Nature Genetics|September 5, 2007
Challenges and standards in integrating surveys of structural variationStephen W Scherer, Charles Lee, Ewan Birney, et al.
Gene|February 5, 1999
The BCL7 gene family: deletion of BCL7B in Williams syndromeD M Jadayel, L R Osborne, L J Coignet, et al.
Human Molecular Genetics|August 1, 1994
Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactylyS W Scherer, P Poorkaj, H Massa, et al.
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