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Clinical Characteristics and Genetic Analysis of a Family With Birt-Hogg-Dubé Syndrome and Congenital Contractural Arachnodactyly
Background: Birt-Hogg-Dubé (BHD) syndrome and congenital contractural arachnodactyly (CCA) or Beals-Hecht syndrome are clinically rare autosomal dominant genetic diseases. In this study, we describe an extremely rare family with BHD syndrome and CCA. Objective: To investigate the clinical and geneti...
Autores principales: | Qiu, Jiayong, Lou, Yao, Zhu, Yingwei, Wang, Min, Peng, Huifang, Hao, Yingying, Jiang, Hongwei, Mao, Yimin |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807514/ https://www.ncbi.nlm.nih.gov/pubmed/35126451 http://dx.doi.org/10.3389/fgene.2021.768342 |
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