Watson, Michael S.
American College of Medical Genetics
5 papers on CoChat
Most cited papers
- Verified
Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies
Miller, D. T., Adam, M. P., Aradhya, S., Biesecker, L. G., Brothman, A. R., Carter, N. P., Church, D. M., Crolla, J. A., Eichler, E. E., Epstein, C. J., et al. (2010) · The American Journal of Human Genetics
Genomic variations and chromosomal abnormalitiesGenomics and Rare Diseases
Cited by 2,882
- Verified
ClinGen — The Clinical Genome Resource
Rehm, H. L., Berg, J. S., Brooks, L. D., Bustamante, C. D., Evans, J. P., Landrum, M. J., Ledbetter, D. H., Maglott, D. R., Martin, C. L., Nussbaum, R. L., et al. (2015) · New England Journal of Medicine
Genomics and Rare DiseasesCardiomyopathy and Myosin Studies
Cited by 1,496
- Verified
Newborn screening: toward a uniform screening panel and system—executive summary
Watson, M. S., Mann, M. Y., Lloyd-Puryear, M. A., Rinaldo, P., Howell, R. R., & American College of Medical Genetics Newborn Screening Expert Group (2006) · Pediatrics
Metabolism and Genetic DisordersGenomics and Rare Diseases
Cited by 494
- Verified
Laboratory standards and guidelines for population-based cystic fibrosis carrier screening
Grody, W. W., Cutting, G. R., Klinger, K. W., Richards, C. S., Watson, M. S., & Desnick, R. J. (2001) · Genetics in Medicine
Cystic Fibrosis Research AdvancesGenomics and Rare Diseases
Cited by 456
- Verified
Main Report
Watson, M. S., Lloyd-Puryear, M. A., Mann, M. Y., Rinaldo, P., & Howell, R. R. (2006) · Genetics in Medicine
Metabolism and Genetic DisordersGenomics and Rare Diseases
Cited by 93
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