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The Journal of Clinical Psychiatry|November 4, 2015
Impact of psychiatric comorbidity and cognitive deficit on function in 22q11.2 deletion syndromeJames J Yi, Monica E Calkins, Sunny X Tang, et al.Clinical Genetics|September 8, 2022
Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expressionIan M Campbell, T Blaine Crowley, Chintan Jobaliya, et al.Schizophrenia Research|July 16, 2018
Olfactory deficits and psychosis-spectrum symptoms in 22q11.2 deletion syndromeSunny X Tang, Paul J Moberg, James J Yi, et al.Journal of the American Academy of Child and Adolescent Psychiatry|August 25, 2014
Subthreshold psychotic symptoms in 22q11.2 deletion syndromeSunny X Tang, James J Yi, Tyler M Moore, et al.Biological Psychiatry|January 4, 2015
Aberrant Cortical Morphometry in the 22q11.2 Deletion SyndromeJ Eric Schmitt, Simon Vandekar, James Yi, et al.Human Genome Variation|June 9, 2016
A catalog of hemizygous variation in 127 22q11 deletion patientsMatthew S Hestand, Beata A Nowakowska, Elfi Vergaelen, et al.Genome Research|September 5, 2019
The 22q11 low copy repeats are characterized by unprecedented size and structural variabilityWolfram Demaerel, Yulia Mostovoy, Feyza Yilmaz, et al.Journal of Medical Genetics|December 13, 2012
Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DSDonna M McDonald-McGinn, Somayyeh Fahiminiya, Timothée Revil, et al.American Journal of Human Genetics|August 3, 2010
A palindrome-mediated recurrent translocation with 3:1 meiotic nondisjunction: the t(8;22)(q24.13;q11.21)Molly B Sheridan, Takema Kato, Chad Haldeman-Englert, et al.Scientific Reports|July 24, 2020
Optical mapping of the 22q11.2DS region reveals complex repeat structures and preferred locations for non-allelic homologous recombination (NAHR)Steven Pastor, Oanh Tran, Andrea Jin, et al.Pageof 14