These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
23. Systemic Hyalinosis With Heterozygous CMG2 Mutations: A Case Report and Review of Literature. Rahvar M; Teng J; Kim J Am J Dermatopathol; 2016 May; 38(5):e60-3. PubMed ID: 26885603 [TBL] [Abstract][Full Text] [Related]
24. Heterogeneity and atypical presentation in infantile systemic hyalinosis with severe labio-gingival enlargement: first Egyptian report. El-Kamah GY; Mostafa MI Dermatol Online J; 2009 May; 15(5):6. PubMed ID: 19624984 [TBL] [Abstract][Full Text] [Related]
25. Hyaline Fibromatosis Syndrome Diagnosed by Whole Genome Sequencing. Anderson S J Pediatr Health Care; 2024 Feb; ():. PubMed ID: 38385928 [TBL] [Abstract][Full Text] [Related]
27. Hyaline fibromatosis syndrome with a novel 4.41-kb deletion in ANTXR2 gene: A case report and literature review. Zhu Y; Du X; Sun L; Wang H; Wang D; Wu B Mol Genet Genomic Med; 2022 Aug; 10(8):e1993. PubMed ID: 35726349 [TBL] [Abstract][Full Text] [Related]
28. Gingival Hypertrophy in a Child with Hyaline Fibromatosis Syndrome. Knežević P; Tarle M; Fratrić LI; Tarle A; Knežević-Krajina H; Macan D Acta Stomatol Croat; 2020 Mar; 54(1):69-74. PubMed ID: 32523159 [TBL] [Abstract][Full Text] [Related]
29. [Infantile systemic hyalinosis: a case report and literature review]. Lu J; Li J; Lin FY Zhonghua Er Ke Za Zhi; 2016 Dec; 54(12):946-949. PubMed ID: 27938598 [No Abstract] [Full Text] [Related]