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2. The Aarskog (facio-digital-genital) syndrome in South Africa. A report of three families. de Saxe M, Kromberg JG, Jenkins T. S Afr Med J; 1984 Feb 25; 65(8):299-303. PubMed ID: 6695301 [Abstract] [Full Text] [Related]
3. Kuwait type faciodigitogenital syndrome. Teebi AS, al Awadi SA. J Med Genet; 1991 Nov 25; 28(11):805. PubMed ID: 1770541 [No Abstract] [Full Text] [Related]
5. Autosomal dominant inheritance of the Aarskog syndrome. Grier RE, Farrington FH, Kendig R, Mamunes P. Am J Med Genet; 1983 May 25; 15(1):39-46. PubMed ID: 6344635 [Abstract] [Full Text] [Related]
6. The inheritance of the Aarskog facial-digital-genital syndrome. Berman P, Desjardins C, Fraser FC. J Pediatr; 1975 Jun 25; 86(6):885-91. PubMed ID: 1127528 [Abstract] [Full Text] [Related]
7. [Aarskog's syndrome. Description of a case and endocrinological study]. Saggese G, Bertelloni S, Baroncelli GI, Calisti L. Pediatr Med Chir; 1983 Jun 25; 5(6):613-8. PubMed ID: 6442411 [Abstract] [Full Text] [Related]
8. Aarskog syndrome in a Brazilian boy born to consanguineous parents. Guion-Almeida ML, Richieri-Costa A. Am J Med Genet; 1992 Jul 15; 43(5):808-10. PubMed ID: 1642267 [Abstract] [Full Text] [Related]
9. [Aarskog's syndrome]. Hromádková L, Frána L. Cesk Oftalmol; 1991 May 15; 47(3):212-8. PubMed ID: 1913912 [Abstract] [Full Text] [Related]
10. [Aarskog syndrome. A case report]. Cincinnati P, Lombardi AM, Morelli M, Rutiloni C. Minerva Pediatr; 1994 Sep 15; 46(9):407-10. PubMed ID: 7799889 [Abstract] [Full Text] [Related]
11. Picture of the month. Stromquist C, Giacoia GP, Feingold M. Am J Dis Child; 1988 Sep 15; 142(9):981-2. PubMed ID: 3414632 [No Abstract] [Full Text] [Related]
12. The facio-digito-genital syndrome (Aarskog syndrome): a further delineation of the distinct radiological findings. Lizcano-Gil LA, Garcia-Cruz D, Cantu JM, Fryns JP. Genet Couns; 1994 Sep 15; 5(4):387-92. PubMed ID: 7888143 [Abstract] [Full Text] [Related]
13. Autosomal recessive Robinow syndrome. Teebi AS. Am J Med Genet; 1990 Jan 15; 35(1):64-8. PubMed ID: 2301471 [Abstract] [Full Text] [Related]
14. The Aarskog syndrome in a large family, suggestive for autosomal dominant inheritance. van de Vooren MJ, Niermeijer MF, Hoogeboom AJ. Clin Genet; 1983 Dec 15; 24(6):439-45. PubMed ID: 6652957 [Abstract] [Full Text] [Related]
15. The Aarskog syndrome. Fryns JP, Macken J, Vinken L, Igodt-Ameye L, van den Berghe H. Hum Genet; 1978 Jun 09; 42(2):129-35. PubMed ID: 669698 [Abstract] [Full Text] [Related]
16. Syndrome of camptodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia--further delineation and evidence for autosomal recessive inheritance. Pena SD, Shokeir MH. Birth Defects Orig Artic Ser; 1976 Jun 09; 12(5):201-8. PubMed ID: 953225 [No Abstract] [Full Text] [Related]
17. A new recessive syndrome of unusual facies, digital abnormalities, and ichthyosis. Clayton-Smith J, Donnai D. J Med Genet; 1989 May 09; 26(5):339-42. PubMed ID: 2732996 [Abstract] [Full Text] [Related]
18. Genetics of the Meckel syndrome (dysencephalia splanchnocystica). Hsia YE, Bratu M, Herbordt A. Pediatrics; 1971 Aug 09; 48(2):237-47. PubMed ID: 4997860 [No Abstract] [Full Text] [Related]
19. [Aarskog's syndrome: variable manifestations in men and women]. Franková Y, Stloukalová M, Rubín A. Cesk Pediatr; 1986 Sep 09; 41(9):535-8. PubMed ID: 3769028 [No Abstract] [Full Text] [Related]