407 Views | 334 Downloads
Correspondence: Susan A. Berry (berry002@umn.edu)
The authors thank the investigators at the following institutions: University of Minnesota Amplatz Children’s Hospital (Kristi Bentler); Cincinnati Children’s Hospital Medical Center (Nancy Leslie); Emory University (Mary Brauchla); Greenwood Genetics Center (Melinda Whetsell and Neena Champaigne); University of Florida (Helen McCune and Robert Zori); University of North Carolina–Chapel Hill (Dianne Frazier); University of Tennessee (Darla Henderson Smith); Vanderbilt University Medical Center (Gina Wey); Mount Sinai Medical Center (Roberta Salveson); Children’s Hospital at Albany Medical Center (Katherine Marra); Children’s Hospital of Pittsburgh (Judith Henry); Golisano Children’s Hospital at Strong (Eileen Blakely); Maria Fareri Children’s Hospital at Westchester Medical Center (Shideh Mofidi); University of Maryland Hospital for Children (Megan Skinner).
The authors declare no conflict of interest.
The project was supported through a Cooperative Agreement between the Maternal and Child Health Bureau (MCHB), Genetic Services Branch, and the University of Texas Health Science Center at San Antonio, National Newborn Screening and Genetics Resource Center, Health Resources and Services Administration (HRSA) grant no. U32MC00148 and by HRSA-MCHB Regional Genetic and Newborn Screening Services Collaboratives, Heritable Disorders Program: Region 2 New York—Mid-Atlantic Consortium for Genetic and Newborn Screening Services, Cooperative Agreement No. U22MC03956; Region 3 Southeast Newborn Screening and Genetics Collaborative, Cooperative Agreement No. U22MC10979; and Region 4 Midwest Genetics Collaborative, Cooperative Agreement No. U22MC03963.
© American College of Medical Genetics and Genomics.