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3. Aarskog syndrome: report of a family with review and discussion of nosology. Teebi AS, Rucquoi JK, Meyn MS. Am J Med Genet; 1993 Jun 15; 46(5):501-9. PubMed ID: 8322809 [Abstract] [Full Text] [Related]
6. [Aarskog's syndrome (facial-digital-genital syndrome). Study of a family (author's transl)]. Scarano G, Rinaldi MM, Cavaliere ML, Esposito M, Sicolo A, Santulli B, Stabile M, Fasano R, Ventruto V. Pediatr Med Chir; 1981 Jun 15; 3(4):323-5. PubMed ID: 7343926 [Abstract] [Full Text] [Related]
7. Aarskog syndrome associated with hypermetropia and toe anomaly. Caksen H, Kurtoğlu S, Ciftçi A, Cağil N, Gikrikçi V. S Afr Med J; 1997 Dec 15; 87(12):1699-700. PubMed ID: 9497838 [Abstract] [Full Text] [Related]
8. Translocation breakpoint in Aarskog syndrome maps to Xp11.21 between ALAS2 and DXS323. Glover TW, Verga V, Rafael J, Barcroft C, Gorski JL, Bawle EV, Higgins JV. Hum Mol Genet; 1993 Oct 15; 2(10):1717-8. PubMed ID: 8268928 [No Abstract] [Full Text] [Related]
11. A novel mutation in a mother and a son with Aarskog-Scott syndrome. Altıncık A, Kaname T, Demir K, Böber E. J Pediatr Endocrinol Metab; 2013 Oct 15; 26(3-4):385-8. PubMed ID: 23443263 [Abstract] [Full Text] [Related]
15. A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanel. Parıltay E, Hazan F, Ataman E, Demir K, Etlik Ö, Özbek E, Özkan B. J Pediatr Endocrinol Metab; 2016 Sep 01; 29(9):1111-4. PubMed ID: 27544718 [Abstract] [Full Text] [Related]