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Neuroimage. Clinical|September 14, 2016
Disrupted anatomic networks in the 22q11.2 deletion syndromeJ Eric Schmitt, James Yi, Monica E Calkins, et al.
Cell|April 10, 2012
A mechanism for gene-environment interaction in the etiology of congenital scoliosisDuncan B Sparrow, Gavin Chapman, Allanceson J Smith, et al.
Human Molecular Genetics|January 1, 1997
Genotype-phenotype correlation for nucleotide substitutions in the IgII-IgIII linker of FGFR2M Oldridge, P W Lunt, E H Zackai, et al.
The American Journal of Psychiatry|September 1, 2004
Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndromeCarrie E Bearden, Abbas F Jawad, David R Lynch, et al.
Molecular Syndromology|July 26, 2013
More Clinical Overlap between 22q11.2 Deletion Syndrome and CHARGE Syndrome than Often AnticipatedN Corsten-Janssen, S C Saitta, L H Hoefsloot, et al.
The Journal of Pediatrics|April 19, 2024
Genomic Contributors to Esophageal Atresia and Tracheoesophageal Fistula: A 12 Year Retrospective ReviewK Taylor Wild, Laura Conlin, Justin Blair, et al.
The Journal of Thoracic and Cardiovascular Surgery|May 18, 2016
Increasing cumulative exposure to volatile anesthetic agents is associated with poorer neurodevelopmental outcomes in children with hypoplastic left heart syndromeLaura K Diaz, J William Gaynor, Shannon J Koh, et al.
American Journal of Medical Genetics. Part A|July 8, 2005
Craniosynostosis: another feature of the 22q11.2 deletion syndromeDonna M McDonald-McGinn, Karen W Gripp, Richard E Kirschner, et al.
Brain and Behavior|July 2, 2021
Relationship between intelligence quotient measures and computerized neurocognitive performance in 22q11.2 deletion syndromeRuben C Gur, Tyler M Moore, Ronnie Weinberger, et al.
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