Chronic tibial nonunion in a Rothmund-Thomson syndrome patient
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35475/fullpdf
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1. Rothmund-Thomson Syndrome-Like RECQL4 Truncating Mutations Cause a Haploinsufficient Low-Bone-Mass Phenotype in Mice;Molecular and Cellular Biology;2021-02-23
2. Rothmund-Thomson Syndrome-like RECQL4 truncating mutations cause a haploinsufficient low bone mass phenotype in mice;2020-11-12
3. Novel pathogenic RECQL4 variants in Chinese patients with Rothmund-Thomson syndrome;Gene;2018-05
4. Generalized metabolic bone disease and fracture risk in Rothmund-Thomson syndrome;Human Molecular Genetics;2017-05-09
5. Delayed Union of a Jones Fracture in a Patient With Rothmund-Thomson Syndrome: A Case Report and Review of the Literature;The Journal of Foot and Ankle Surgery;2016-03
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