A fragile X sibship from a consanguineous family with a compound heterozygous female and partially methylated full mutation male

Abstract

American Journal of Medical Genetics Part AVolume 158A, Issue 5 p. 1221-1224 Research Letter A fragile X sibship from a consanguineous family with a compound heterozygous female and partially methylated full mutation male†‡ Page L. Sorensen, Page L. Sorensen MIND Institute, University of California at Davis Medical Center, Sacramento, California Department of Pediatrics, University of California at Davis Medical Center, Sacramento, CaliforniaSearch for more papers by this authorKirin Basuta, Kirin Basuta Department of Biochemistry and Molecular Medicine, University of California at Davis, School of Medicine, Davis, CaliforniaSearch for more papers by this authorGuadalupe Mendoza-Morales, Guadalupe Mendoza-Morales Department of Biochemistry and Molecular Medicine, University of California at Davis, School of Medicine, Davis, CaliforniaSearch for more papers by this authorLouise W. Gane, Louise W. Gane MIND Institute, University of California at Davis Medical Center, Sacramento, California Department of Pediatrics, University of California at Davis Medical Center, Sacramento, CaliforniaSearch for more papers by this authorAndrea Schneider, Andrea Schneider MIND Institute, University of California at Davis Medical Center, Sacramento, CaliforniaSearch for more papers by this authorRandi Hagerman, Randi Hagerman MIND Institute, University of California at Davis Medical Center, Sacramento, California Department of Pediatrics, University of California at Davis Medical Center, Sacramento, CaliforniaSearch for more papers by this authorFlora Tassone, Corresponding Author Flora Tassone [email protected] MIND Institute, University of California at Davis Medical Center, Sacramento, California Department of Biochemistry and Molecular Medicine, University of California at Davis, School of Medicine, Davis, CaliforniaDepartment of Biochemistry and Molecular Medicine, University of California Davis, Oak Park Research Building, Suite 102, 2700 Stockton Blvd, Sacramento, CA 95817; MIND Institute Wet Lab, 2805 50th Street Room 2460, Sacramento, CA 95817.Search for more papers by this author Page L. Sorensen, Page L. Sorensen MIND Institute, University of California at Davis Medical Center, Sacramento, California Department of Pediatrics, University of California at Davis Medical Center, Sacramento, CaliforniaSearch for more papers by this authorKirin Basuta, Kirin Basuta Department of Biochemistry and Molecular Medicine, University of California at Davis, School of Medicine, Davis, CaliforniaSearch for more papers by this authorGuadalupe Mendoza-Morales, Guadalupe Mendoza-Morales Department of Biochemistry and Molecular Medicine, University of California at Davis, School of Medicine, Davis, CaliforniaSearch for more papers by this authorLouise W. Gane, Louise W. Gane MIND Institute, University of California at Davis Medical Center, Sacramento, California Department of Pediatrics, University of California at Davis Medical Center, Sacramento, CaliforniaSearch for more papers by this authorAndrea Schneider, Andrea Schneider MIND Institute, University of California at Davis Medical Center, Sacramento, CaliforniaSearch for more papers by this authorRandi Hagerman, Randi Hagerman MIND Institute, University of California at Davis Medical Center, Sacramento, California Department of Pediatrics, University of California at Davis Medical Center, Sacramento, CaliforniaSearch for more papers by this authorFlora Tassone, Corresponding Author Flora Tassone [email protected] MIND Institute, University of California at Davis Medical Center, Sacramento, California Department of Biochemistry and Molecular Medicine, University of California at Davis, School of Medicine, Davis, CaliforniaDepartment of Biochemistry and Molecular Medicine, University of California Davis, Oak Park Research Building, Suite 102, 2700 Stockton Blvd, Sacramento, CA 95817; MIND Institute Wet Lab, 2805 50th Street Room 2460, Sacramento, CA 95817.Search for more papers by this author First published: 09 April 2012 https://doi.org/10.1002/ajmg.a.35293Citations: 7 † This work is dedicated to the memory of Matteo. ‡ How to Cite this Article: Sorensen PL, Basuta K, Mendoza-Morales G, Gane LW, Schneider A, Hagerman R, Tassone F. 2012. A fragile X sibship from a consanguineous family with a compound heterozygous female and partially methylated full mutation male. Am J Med Genet Part A. 158A:1221–1224. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Citing Literature Volume158A, Issue5May 2012Pages 1221-1224 RelatedInformation