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3. [Defects of the femur and fibula with amelia, peromelia or ulnar defects of the arm. A syndrome]. Kühne D; Lenz W; Petersen D; Schönenberg H Humangenetik; 1967; 3(3):244-63. PubMed ID: 6074386 [No Abstract] [Full Text] [Related]
4. A case of femur-fibular-ulna complex with peculiar metaphyseal changes. Ludwig K; Tenconi R; Salmaso R Fetal Pediatr Pathol; 2010; 29(4):255-60. PubMed ID: 20594150 [TBL] [Abstract][Full Text] [Related]
5. Absence of fibula and ulna with oligodactyly, contractures, right-angle bowing of femora, abnormal facial morphology, cleft lip/palate and brain malformation in two sibs: a possibly new lethal syndrome. Pfeiffer RA; Stöss H; Voight HJ; Wündisch GF Am J Med Genet; 1988 Apr; 29(4):901-8. PubMed ID: 3400735 [TBL] [Abstract][Full Text] [Related]
6. [Femur-fibula-ulna (FFU) complex in the 33rd week of gestation: ultrasonography, radiology, pathology and differential diagnosis. Case report]. Guschmann M; Becker R; Urban M; Entezami M; Hese S; Vogel M Klin Padiatr; 2001; 213(5):301-5. PubMed ID: 11582532 [TBL] [Abstract][Full Text] [Related]
8. The femur, fibula, ulna (FFU) complex in siblings. Zlotogora J; Rosenmann E; Menashe M; Robin GC; Cohen T Clin Genet; 1983 Dec; 24(6):449-52. PubMed ID: 6652959 [TBL] [Abstract][Full Text] [Related]
9. Causal study of isolated ulnar-fibular deficiency in Hungary, 1975-1984. Czeizel AE; Vitéz M; Kodaj I; Lenz W Am J Med Genet; 1993 Jun; 46(4):427-33. PubMed ID: 8357016 [TBL] [Abstract][Full Text] [Related]
10. [Congenital skeletal limb deficiencies. Examples and their treatment]. Seyhan F; Ahiskali G Turk Tip Cemiy Mecm; 1972 Nov; 38(11):481-8. PubMed ID: 4668355 [No Abstract] [Full Text] [Related]
11. Ultrasound-guided interscalene brachial plexus block in a child with femur fibula ulna syndrome. Jan van Geffen G; Tielens L; Gielen M Paediatr Anaesth; 2006 Mar; 16(3):330-2. PubMed ID: 16490101 [TBL] [Abstract][Full Text] [Related]
12. Familial aplasia/hypoplasia of pelvis, femur, fibula, and ulna with abnormal digits in an inbred Pakistani Muslim family: a possible new autosomal recessive disorder with overlapping manifestations of the syndromes of Fuhrmann, Al-Awadi, and Raas-Rothschild. Kumar D; Duggan MB; Mueller RF; Karbani G Am J Med Genet; 1997 May; 70(2):107-13. PubMed ID: 9128926 [TBL] [Abstract][Full Text] [Related]
16. FFU complex: an analysis of 491 cases. Lenz W; Zygulska M; Horst J Hum Genet; 1993 May; 91(4):347-56. PubMed ID: 8500790 [TBL] [Abstract][Full Text] [Related]
17. Fibular aplasia with ectrodactyly--broadening the clinical spectrum. Gieruszczak-Bialek D; Oldak M; Skorka A; Waligora J; Korniszewski L Eur J Med Genet; 2006; 49(1):83-6. PubMed ID: 16473314 [TBL] [Abstract][Full Text] [Related]
18. 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 [TBL] [Abstract][Full Text] [Related]
19. Prenatal ultrasound diagnosis of a femur-fibula-ulna complex during the first half of pregnancy. Florio I; Wisser J; Huch R; Huch A Fetal Diagn Ther; 1999; 14(5):310-2. PubMed ID: 10529577 [TBL] [Abstract][Full Text] [Related]
20. Severity of ulnar deficiency and its relationship with lower extremity deficiencies. Walker JL; Hosseinzadeh P; Lea J; White H; Bell S; Riley SA J Pediatr Orthop B; 2019 Jan; 28(1):62-66. PubMed ID: 30204624 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]