Work Groups

Quality Assurance Products

Lab Quality and Follow-Up in the New England Genetics Collaborative

link by Eaton, Roger, PhD; Comeau, Anne, PhD., Sahai, Inderneel, MD; NCC Collaborator, December 2009

Quality Assurance Publications

The increased incidence of congenital hypothyroidism: Fact or fancy?

Link By Mitchell, M.L., Hsu, H.W., Sahai, I., & Massachusetts Pediatric Endocrine Work Group Clinical Endocrinology, 2011;75(6), 806-10
A near-miss: very long chain acyl-CoA dehydrogenase deficiency with normal primary markers in the initial well-timed newborn screening specimen.

Link by Sahai, I., Bailey, J.C., Eaton, R.B., Zytkovicz, T., & Harris, D.J. Journal of Pediatrics, 2011;1(1), 172.
Spectrum of Medium Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency detected by newborn screening.

link by Hsu H-W, Zytkovicz TH, Comeau, AM, Strauss AW, Marsden D, Shih VE, Grady GF and Eaton RB; Pediatrics, 2008;121:e1108-e1114

Contact
The New England
Genetics Collaborative
10 West Edge Drive
Suite 101, Durham, NH 03284
Email: Contact Us
Phone: 603-862-4320
Fax: 603-862-0555

The New England Genetics Collaborative is funded by Cooperative Agreement No. U22MC10980 between the University of New Hampshire and the Health Resources and Services Administration/ Maternal and Child Health Bureau/DSCSHN Genetic Services Branch.