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For: Boothe M, Morris R, Robin N. Stickler Syndrome: A Review of Clinical Manifestations and the Genetics Evaluation. J Pers Med 2020;10:E105. [PMID: 32867104 DOI: 10.3390/jpm10030105] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 2.5] [Reference Citation Analysis]
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1 Van Heurck R, Carminho-Rodrigues MT, Ranza E, Stafuzza C, Quteineh L, Gehrig C, Hammar E, Guipponi M, Abramowicz M, Senn P, Guinand N, Cao-Van H, Paoloni-Giacobino A. Benefits of Exome Sequencing in Children with Suspected Isolated Hearing Loss. Genes (Basel) 2021;12:1277. [PMID: 34440452 DOI: 10.3390/genes12081277] [Reference Citation Analysis]
2 Moshirfar M, Barke MR, Huynh R, Waite AJ, Ply B, Ronquillo YC, Hoopes PC. Controversy and Consideration of Refractive Surgery in Patients with Heritable Disorders of Connective Tissue. J Clin Med 2021;10:3769. [PMID: 34501218 DOI: 10.3390/jcm10173769] [Reference Citation Analysis]
3 Apgar TL, Sanders CR. Compendium of causative genes and their encoded proteins for common monogenic disorders. Protein Sci 2021. [PMID: 34515378 DOI: 10.1002/pro.4183] [Reference Citation Analysis]
4 Baiyasi A, Barbosa J, Parendo A, Lin X. Pleiotropy of a Stickler syndrome genotype. Eur J Ophthalmol 2021;:11206721211035611. [PMID: 34313156 DOI: 10.1177/11206721211035611] [Reference Citation Analysis]
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