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Circulation|July 31, 2002
Fetal cardiomyopathies: pathogenic mechanisms, hemodynamic findings, and clinical outcomeSimone R F F Pedra, Jeffrey F Smallhorn, Greg Ryan, et al.
The Journal of Clinical Endocrinology and Metabolism|November 12, 2014
Type V OI primary osteoblasts display increased mineralization despite decreased COL1A1 expressionAdi Reich, Alison S Bae, Aileen M Barnes, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 30, 2013
Genotype-phenotype correlation in 1,507 families with congenital adrenal hyperplasia owing to 21-hydroxylase deficiencyMaria I New, Moolamannil Abraham, Brian Gonzalez, et al.
Journal of Neurosurgery. Pediatrics|January 31, 2015
Postshunt lateral ventricular volume, white matter integrity, and intellectual outcomes in spina bifida and hydrocephalusVictoria J Williams, Jenifer Juranek, Karla K Stuebing, et al.
The American Journal of Psychiatry|August 17, 2018
Risk of Major Malformations in Infants Following First-Trimester Exposure to QuetiapineLee S Cohen, Lina Góez-Mogollón, Alexandra Z Sosinsky, et al.
American Journal of Human Genetics|May 13, 2003
Mutations in the transcription factor gene SOX18 underlie recessive and dominant forms of hypotrichosis-lymphedema-telangiectasiaAlexandre Irrthum, Koenraad Devriendt, David Chitayat, et al.
Genome Medicine|April 4, 2009
The cycle of genome-directed medicineJanet A Buchanan, Andrew R Carson, David Chitayat, et al.
AJNR. American Journal of Neuroradiology|July 1, 2026
Comprehensive Structural MRI Phenotyping in Oligophrenin 1-Related Disorder Reveals Characteristic Brain MalformationsAsthik Biswas, Matthew T Whitehead, Parthiv Haldipur, et al.
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