Gnathodiaphyseal dysplasia with a novel R597I mutation of ANO5: Mandibular reconstruction strategies-Reference-Cited by-同舟云学术

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Gnathodiaphyseal dysplasia with a novel R597I mutation of ANO5: Mandibular reconstruction strategies

Published:2019-11 Issue:5 Volume:120 Page:428-431
ISSN:2468-7855
Container-title:Journal of Stomatology, Oral and Maxillofacial Surgery
language:en
Short-container-title:Journal of Stomatology, Oral and Maxillofacial Surgery

Author:

Marechal G.,Schouman T.,Mauprivez C.,Benassarou M.,Chaine A.,Diner P.-A.,Zazurca F.,Soupre V.,Michot C.,Baujat G.,Khonsari R.H.

Publisher

Elsevier BV

Subject

Otorhinolaryngology,Oral Surgery,Surgery

Reference17 articles.

1. Gnathodiaphyseal dysplasia: a syndrome of fibro-osseous lesions of jawbones, bone fragility, and long bone bowing;Riminucci;J Bone Miner Res,2001

2. Recurring gnathodiaphyseal dysplasia in two Russian brothers;Roginsky;Int J Oral Maxillofac Surg,2010

3. Autosomal dominant gnathodiaphyseal dysplasia maps to chromosome 11p14.3-15.1;Tsutsumi;J Bone Miner Res,2003

4. The novel gene encoding a putative transmembrane protein is mutated in gnathodiaphyseal dysplasia (GDD);Tsutsumi;Am J Hum Genet,2004

5. Three novel ANO5 missense mutations in Caucasian and Chinese families and sporadic cases with gnathodiaphyseal dysplasia;Jin;Sci Rep,2017

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Craniofacial disorders and dysplasias: Molecular, clinical, and management perspectives;Bone Reports;2024-03

2. Integration of metabolomics and transcriptomics provides insights into enhanced osteogenesis in Ano5Cys360Tyr knock-in mouse model;Frontiers in Endocrinology;2023-01-20

3. Gnathodiaphyseal dysplasia with a novel genetic variant in a large family from Iran;Molecular Genetics & Genomic Medicine;2022-06-27

4. Displasia gnatodiafisaria: revisione della letteratura e trattamento di due casi clinici;Dental Cadmos;2021-04

5. ANO5 ‐associated Gnathodiaphyseal dysplasia with calvarial doughnut lesions: First report in an Asian Indian with an expanded phenotype;Congenital Anomalies;2020-09-15

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