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2. Prenatal diagnosis of femur-fibula-ulna complex by ultrasonography in a male fetus at 24 weeks of gestation. Capece G, Fasolino A, Della Monica M, Lonardo F, Scarano G, Neri G. Prenat Diagn; 1994 Jun; 14(6):502-5. PubMed ID: 7937589 [Abstract] [Full Text] [Related]
5. A case of femur-fibular-ulna complex with peculiar metaphyseal changes. Ludwig K, Tenconi R, Salmaso R. Fetal Pediatr Pathol; 2010 Jun; 29(4):255-60. PubMed ID: 20594150 [Abstract] [Full Text] [Related]
9. A local outbreak of femoral hypoplasia or aplasia and femoral fibula-ulnar-complex. Robert JM, Guibaud P, Robert E. J Genet Hum; 1981 Dec; 29(4):379-94. PubMed ID: 7328413 [Abstract] [Full Text] [Related]
11. Severe hypoplasia of the right femur, ipsilateral agenesia of the fibula and twisted right foot in a 24-week-old fetus with proximal femoral focal deficiency (PFFD). La Torre R, Mastrone M, Coacci F, Labi L, Palma E, Di Giusto M, Patella A, Cosmi EV. Clin Exp Obstet Gynecol; 2003 Dec; 30(1):65-6. PubMed ID: 12731749 [Abstract] [Full Text] [Related]
12. Proximal focal femoral deficiency, contralateral hip dysplasia in association with contralateral ulnar hypoplasia and clefthand: a case report and review of literatures of PFFD and/or FFU. Kalaycioglu A, Aynaci O. Okajimas Folia Anat Jpn; 2001 Aug; 78(2-3):83-9. PubMed ID: 11732209 [Abstract] [Full Text] [Related]
14. Craniosynostosis with wormian bone, bowing of the long bones, unilateral short femur, and focal fibula deficiency: a prenatal diagnostic dilemma. Tonni G, Lituania M, Rosignoli L. J Clin Ultrasound; 2013 Sep; 41(7):448-52. PubMed ID: 23090838 [Abstract] [Full Text] [Related]
15. Bilateral ulna hypoplasia, club feet, and mental retardation: a new mesomelic syndrome. Kohn G, Malinger G, el Shawwa R, Scheinfeld A, Tepper R, Ornoy A, Lachman R, Rimoin DL. Am J Med Genet; 1995 Mar 27; 56(2):132-5. PubMed ID: 7625433 [Abstract] [Full Text] [Related]
16. Unilateral and asymmetric limb defects in man: delineation of the femur-fibula-ulna complex. Lenz W, Feldmann U. Birth Defects Orig Artic Ser; 1977 Mar 27; 13(1):269-85. PubMed ID: 851600 [No Abstract] [Full Text] [Related]
18. Two sporadic cases of amelia/phocomelia with similar phenotype: rare and unusually symmetrical form of FFU dysostosis or separate entity? Kardon NB, Dana LP, FitzGerald JM, Opitz JM. Am J Med Genet Suppl; 1986 Mar 27; 2():239-45. PubMed ID: 3146295 [Abstract] [Full Text] [Related]