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Fetal and Pediatric Pathology Volume 35, 2016 - Issue 5
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CASE REPORT

Novel FKBP10 Mutation in a Patient with Osteogenesis Imperfecta Type XI

Seyed Mohammad SeyedhassaniGenomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran;Dr. Seyedhassani Medical Genetic Center, Yazd, IranCorrespondence[email protected]
,
Feyzollah Hashemi-GorjiGenomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
,
Mahdieh YavariDr. Seyedhassani Medical Genetic Center, Yazd, Iran
,
Fahimeh HaraziDr. Seyedhassani Medical Genetic Center, Yazd, Iran
&
Vahid Reza YassaeeGenomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Pages 353-358 | Received 22 Mar 2016, Accepted 10 May 2016, Published online: 30 Jun 2016

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Read on this site (1)

Harvy Mauricio Velasco & Jessica L Morales. (2017) Novel mutation of FKBP10 in a pediatric patient with osteogenesis imperfecta type XI identified by clinical exome sequencing. The Application of Clinical Genetics 10, pages 75-83.
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Articles from other publishers (1)

嘉欣 袁. (2023) Research Advances in Genetic on Osteogenesis Imperfecta. Advances in Clinical Medicine 13:06, pages 9417-9425.
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