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9. Acromegaloid facial appearance: case report and literature review. Ghazi A; Khosla S; Becker K Case Rep Endocrinol; 2013; 2013():970396. PubMed ID: 23533839 [TBL] [Abstract][Full Text] [Related]
10. Acromegaloid facial appearance syndrome: a further case report. Kini U; Clayton-Smith J Clin Dysmorphol; 2004 Oct; 13(4):251-253. PubMed ID: 15365463 [TBL] [Abstract][Full Text] [Related]
11. A new case of acromegaloid facial appearance (AFA) syndrome with an expanded phenotype. Zelante L; Gasparini P; Savoia A; Lomuto M; Pellicano R Clin Dysmorphol; 2000 Jul; 9(3):221-2. PubMed ID: 10955485 [TBL] [Abstract][Full Text] [Related]
12. Acromegaloid facial appearance (AFA) syndrome: report of a second family. Dallapiccola B; Zelante L; Accadia L; Mingarelli R J Med Genet; 1992 Jun; 29(6):419-22. PubMed ID: 1619638 [TBL] [Abstract][Full Text] [Related]
14. Cantú syndrome versus Zimmermann-Laband syndrome: Report of nine individuals with ABCC9 variants. Kortüm F; Niceta M; Magliozzi M; Dumic Kubat K; Robertson SP; Moresco A; Dentici ML; Baban A; Leoni C; Onesimo R; Obregon MG; Digilio MC; Zampino G; Novelli A; Tartaglia M; Kutsche K Eur J Med Genet; 2020 Sep; 63(9):103996. PubMed ID: 32622958 [TBL] [Abstract][Full Text] [Related]
15. Idiopathic gingival hyperplasia and hypertrichosis associated with acromegaloid features. Vontobel F Helv Paediatr Acta; 1973 Nov; 28(5):401-11. PubMed ID: 4773221 [No Abstract] [Full Text] [Related]
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17. Hypertrichosis, pigmentary retinopathy, and facial anomalies: a new syndrome? Pivnick EK; Wilroy RS; Martens PR; Teather TC; Hashimoto K Am J Med Genet; 1996 Apr; 62(4):386-90. PubMed ID: 8723069 [TBL] [Abstract][Full Text] [Related]
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19. Cantú syndrome resulting from activating mutation in the KCNJ8 gene. Cooper PE; Reutter H; Woelfle J; Engels H; Grange DK; van Haaften G; van Bon BW; Hoischen A; Nichols CG Hum Mutat; 2014 Jul; 35(7):809-13. PubMed ID: 24700710 [TBL] [Abstract][Full Text] [Related]
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