Fragile X–related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study
Year: 2012
Type: article
Study design: Observational Study
Source: Genetics in Medicine
DOI: 10.1038/gim.2012.134
Authors: Yoshimi Inaba, Amy S. Herlihy, Charles E. Schwartz, Cindy Skinner, Quang M. Bui, Joanna Cobb, Elva Z. Shi, David Francis, Alison Arvaj, David J. Amor, Kate Pope, Tiffany Wotton, Jonathan Cohen, Jacqueline K. Hewitt, Randi J. Hagerman, Sylvia A. Metcalfe, John L. Hopper, Danuta Z. Loesch, Howard R. Slater, David E. Godler
Institutions: Royal Children's Hospital, Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Greenwood Genetic Center, American College of Medical Genetics, The University of Melbourne, Children's Hospital at Westmead, Monash University, University of California Davis Medical Center, University of California, Davis, La Trobe University
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: bronze
OpenAlex ID: W2012500458