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Abstract

Journal Article A deletion hot-spot in exon 7 of the G8α gene (GNAS1) in patients with Aibright hereditary osteodystrophy Get access Shuhua Yu, Shuhua Yu Search for other works by this author on: Oxford Academic PubMed Google Scholar Dawen Yu, Dawen Yu Search for other works by this author on: Oxford Academic PubMed Google Scholar Bryan E. Hainline, Bryan E. Hainline 1Department of Pediatrics, Indiana UniversityIndianapolis, IN 46202 Search for other works by this author on: Oxford Academic PubMed Google Scholar Jacob L. Brener, Jacob L. Brener 2Metropolitan Hospital, New York Medical CollegeNew York, NY 10029 Search for other works by this author on: Oxford Academic PubMed Google Scholar Kathryn Wilson, Kathryn Wilson 3Carle ClinicUrbana, IL 61801, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar Louise C. Wilson, Louise C. Wilson 4Department of Medicine and Therapeutics and Genetics, University of LeicesterLeicester LE1 7RH, UK Search for other works by this author on: Oxford Academic PubMed Google Scholar Monique Oude-Luttikhuls, Monique Oude-Luttikhuls 4Department of Medicine and Therapeutics and Genetics, University of LeicesterLeicester LE1 7RH, UK Search for other works by this author on: Oxford Academic PubMed Google Scholar Richard C. Trembath, Richard C. Trembath 4Department of Medicine and Therapeutics and Genetics, University of LeicesterLeicester LE1 7RH, UK Search for other works by this author on: Oxford Academic PubMed Google Scholar Lee S. Weinstein Lee S. Weinstein * *To whom coerespondence should be addressed at: Metabolic Diseases Branch, NTDDK/NIH, Building 10, Room 8C101, Bethesda, MD 20892-1752, USA Search for other works by this author on: Oxford Academic PubMed Google Scholar Human Molecular Genetics, Volume 4, Issue 10, October 1995, Pages 2001–2002, https://doi.org/10.1093/hmg/4.10.2001 Published: 01 October 1995 Article history Received: 09 June 1995 Revision received: 30 June 1995 Accepted: 30 June 1995 Published: 01 October 1995