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Molecular Autism|May 10, 2016
22q11.2 duplication syndrome: elevated rate of autism spectrum disorder and need for medical screeningTara L Wenger, Judith S Miller, Lauren M DePolo, et al.
American Journal of Medical Genetics. Part A|November 1, 2018
The impact of hypocalcemia on full scale IQ in patients with 22q11.2 deletion syndromeKatheryn Grand, Lorraine E Levitt Katz, T Blaine Crowley, et al.
JAMA Psychiatry|May 19, 2021
Association of Mitochondrial Biogenesis With Variable Penetrance of SchizophreniaJianping Li, Oanh T Tran, T Blaine Crowley, et al.
Cancer Genetics|May 13, 2014
Analysis of the t(3;8) of hereditary renal cell carcinoma: a palindrome-mediated translocationTakema Kato, Colleen P Franconi, Molly B Sheridan, et al.
American Journal of Medical Genetics. Part A|March 9, 2005
The 22q11.2 deletion in African-American patients: an underdiagnosed population?Donna M McDonald-McGinn, Nancy Minugh-Purvis, Richard E Kirschner, et al.
Psychiatry Research|December 28, 2024
Sleep difficulties related to psychopathology and neurocognition in people with 22q11.2 deletion syndromeMargaret C Souders, Donna M McDonald-McGinn, Kosha Ruparel, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 21, 2006
Velopharyngeal anatomy in 22q11.2 deletion syndrome: a three-dimensional cephalometric analysisRachel A Ruotolo, Nestor A Veitia, Aaron Corbin, et al.
Brain and Cognition|May 21, 2016
Performance on a computerized neurocognitive battery in 22q11.2 deletion syndrome: A comparison between US and Israeli cohortsJames J Yi, Ronnie Weinberger, Tyler M Moore, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2006
High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arraysAlexander Eckehart Urban, Jan O Korbel, Rebecca Selzer, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2019
Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive conditionMarta Unolt, Molka Kammoun, Beata Nowakowska, et al.
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