Joint laxity in homozygotes for severePOU1F1mutations

American Journal of Medical Genetics Part AVolume 170, Issue 12 p. 3356-3358 Research Letter Joint laxity in homozygotes for severe POU1F1 mutations Hanan E. Shamseldin, Hanan E. Shamseldin Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi ArabiaSearch for more papers by this authorSateesh Maddirevula, Sateesh Maddirevula Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi ArabiaSearch for more papers by this authorAmira Nabil, Amira Nabil Department of Human Genetics, Medical Research Institute, Alexandria University, Alexandria, EgyptSearch for more papers by this authorSaeed Al-Fadhil, Saeed Al-Fadhil Department of Pediatrics, Armed Forces Hospitals Southern Region, Khamis Mushayt, Saudi ArabiaSearch for more papers by this authorSaeed Al Tala, Saeed Al Tala Department of Pediatrics, Armed Forces Hospitals Southern Region, Khamis Mushayt, Saudi ArabiaSearch for more papers by this authorFowzan S. Alkuraya, Corresponding Author Fowzan S. Alkuraya falkuraya@kfshrc.edu.sa Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia Correspondence to: Fowzan S. Alkuraya, M.D., Department of Genetics, King Faisal Specialist Hospital and Research Center, MBC-03 PO BOX 3354, Riyadh 11211, Saudi Arabia. E-mail: falkuraya@kfshrc.edu.saSearch for more papers by this author Hanan E. Shamseldin, Hanan E. Shamseldin Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi ArabiaSearch for more papers by this authorSateesh Maddirevula, Sateesh Maddirevula Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi ArabiaSearch for more papers by this authorAmira Nabil, Amira Nabil Department of Human Genetics, Medical Research Institute, Alexandria University, Alexandria, EgyptSearch for more papers by this authorSaeed Al-Fadhil, Saeed Al-Fadhil Department of Pediatrics, Armed Forces Hospitals Southern Region, Khamis Mushayt, Saudi ArabiaSearch for more papers by this authorSaeed Al Tala, Saeed Al Tala Department of Pediatrics, Armed Forces Hospitals Southern Region, Khamis Mushayt, Saudi ArabiaSearch for more papers by this authorFowzan S. Alkuraya, Corresponding Author Fowzan S. Alkuraya falkuraya@kfshrc.edu.sa Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh, Saudi Arabia Correspondence to: Fowzan S. Alkuraya, M.D., Department of Genetics, King Faisal Specialist Hospital and Research Center, MBC-03 PO BOX 3354, Riyadh 11211, Saudi Arabia. E-mail: falkuraya@kfshrc.edu.saSearch for more papers by this author First published: 19 August 2016 https://doi.org/10.1002/ajmg.a.37941Citations: 2 Hanan E. Shamseldin and Sateesh Maddirevula contributed equally to this work. Conflicts of interest: Authors declare no conflict of interest. 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 Share a linkShare onFacebookTwitterLinkedInRedditWechat Citing Literature Volume170, Issue12December 2016Pages 3356-3358 RelatedInformation