Irons, Mira

Defective cholesterol biosynthesis associated with the Smith-Lemli-Opitz syndrome

Tint, G. S., Irons, M., Elias, E. R., Batta, A. K., Frieden, R., Chen, T. S., & Salen, G. (1994) · New England Journal of Medicine

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Defective cholesterol biosynthesis in Smith-Lemli-Opitz syndrome

Irons, M., Roy Elias, E., Salen, G., Tint, G. S., & Batta, A. (1993) · The Lancet

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The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Redin, C., Brand, H., Collins, R. L., Kammin, T., Mitchell, E., Hodge, J. C., Hanscom, C., Pillalamarri, V., Seabra, C. M., Abbott, M.-A., et al. (2017) · Nature Genetics

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22q13.3 deletion syndrome: clinical and molecular analysis using array CGH

Dhar, S. U., del Gaudio, D., German, J. R., Peters, S. U., Ou, Z., Bader, P. I., Berg, J. S., Blazo, M., Brown, C. W., Graham, B. H., et al. (2010) · American Journal of Medical Genetics Part A

Genomic variations and chromosomal abnormalitiesGenetics and Neurodevelopmental Disorders

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Trustworthy Augmented Intelligence in Health Care

Crigger, E., Reinbold, K., Hanson, C., Kao, A., Blake, K., & Irons, M. (2022) · Journal of Medical Systems

Artificial Intelligence in Healthcare and EducationEthics and Social Impacts of AI

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MRI and 1H MRS findings in Smith-lemli-opitz syndrome

Caruso, P. A., Poussaint, T. Y., Tzika, A. A., Zurakowski, D., Astrakas, L. G., Elias, E. R., Bay, C., & Irons, M. B. (2004) · Neuroradiology

Metabolism and Genetic DisordersFetal and Pediatric Neurological Disorders

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