A deletion hot-spot in exon 7 of the G8α gene (GNAS1) in patients with aibright hereditary osteodystrophy

Shuhua Yu, Dawen Yu, Bryan E. Hainline, Jacob L. Brener, Kathryn Wilson, Louise C. Wilson, Monique Oude-luttikhuls, Richard C. Trembath, Lee S. Weinstein

Research output: Contribution to journalArticle

56 Scopus citations
Original languageEnglish (US)
Pages (from-to)2001-2002
Number of pages2
JournalHuman molecular genetics
Volume4
Issue number10
DOIs
StatePublished - Oct 1 1995

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

Cite this

Yu, S., Yu, D., Hainline, B. E., Brener, J. L., Wilson, K., Wilson, L. C., Oude-luttikhuls, M., Trembath, R. C., & Weinstein, L. S. (1995). A deletion hot-spot in exon 7 of the G8α gene (GNAS1) in patients with aibright hereditary osteodystrophy. Human molecular genetics, 4(10), 2001-2002. https://doi.org/10.1093/hmg/4.10.2001