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Cerebral Cortex (New York, N.Y. : 1991)|May 17, 2008
Alterations in midline cortical thickness and gyrification patterns mapped in children with 22q11.2 deletionsCarrie E Bearden, Theo G M van Erp, Rebecca A Dutton, et al.
Journal of Psychiatric Research|April 24, 2021
A binational study assessing risk and resilience factors in 22q11.2 deletion syndromeRaquel E Gur, Lauren K White, Shachar Shani, et al.
The Journal of Thoracic and Cardiovascular Surgery|November 26, 2005
Effect of congenital heart disease on neurodevelopmental outcomes within multiple-gestation birthsAmy H Schultz, Gail P Jarvik, Gil Wernovsky, et al.
Journal of the American College of Cardiology|August 26, 1998
Frequency of 22q11 deletions in patients with conotruncal defectsE Goldmuntz, B J Clark, L E Mitchell, et al.
American Journal of Human Genetics|February 11, 1999
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndromeM Oldridge, E H Zackai, D M McDonald-McGinn, et al.
International Journal of Pediatric Otorhinolaryngology|November 6, 2012
A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patientsJosine C C Widdershoven, Mark Bowser, Molly B Sheridan, et al.
The Journal of Thoracic and Cardiovascular Surgery|January 10, 2006
The relationship of postoperative electrographic seizures to neurodevelopmental outcome at 1 year of age after neonatal and infant cardiac surgeryJ William Gaynor, Gail P Jarvik, Judy Bernbaum, et al.
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