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PubMed for id: 816348

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Page 1
Hutchinson-Gilford Progeria syndrome: Report of the first Togolese case.
Guedenon KM, Doubaj Y, Akolly DAE, Barry Moussa W, Saka B, Adjenou K, Belo M, Pio M, Mihluedo-Agbolan KA, Vonor K, Amedome KM, Tchaou M, Atakouma YD, Gbadoe AD, Dossou CF, Fiawoo M, Gnassingbe K, Pitche P, Agbèrè DA, Gnamey DK. Guedenon KM, et al. Am J Med Genet A. 2020 Jun;182(6):1316-1320. doi: 10.1002/ajmg.a.61581. Epub 2020 Apr 16. Am J Med Genet A. 2020. PMID: 32297714
A case of brachyolmia.
Karabiyik N, Oğuz F, Sidal M, Hekim N, Kayserili H. Karabiyik N, et al. Turk J Pediatr. 1997 Jul-Sep;39(3):415-20. Turk J Pediatr. 1997. PMID: 9339123
A family of Melnick-Needles syndrome: a case report.
Oh CH, Lee CH, Kim SY, Lee SY, Jun HH, Lee S. Oh CH, et al. BMC Pediatr. 2020 Aug 19;20(1):391. doi: 10.1186/s12887-020-02288-2. BMC Pediatr. 2020. PMID: 32814550 Free PMC article.
12 results