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Journal Abstract Search

108 related items for PubMed ID: 3895927

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  • 2. 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
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  • 3. New type of autosomal recessive short-limb dwarfism with absent fibulae, exceptionally short digits, and normal intelligence.
    Kohn G, Veder M, Schoenfeld A, el Shawwa R.
    Am J Med Genet; 1989 Dec; 34(4):535-40. PubMed ID: 2624264
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  • 4. Fibular aplasia with ectrodactyly--broadening the clinical spectrum.
    Gieruszczak-Bialek D, Oldak M, Skorka A, Waligora J, Korniszewski L.
    Eur J Med Genet; 2006 Dec; 49(1):83-6. PubMed ID: 16473314
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  • 7. A male newborn infant with fatco syndrome (fibular aplasia, tibial campomelia and oligodactyly): a case report.
    Karaman A, Kahveci H.
    Genet Couns; 2010 Dec; 21(3):285-8. PubMed ID: 20964118
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  • 12. [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 Dec; 213(5):301-5. PubMed ID: 11582532
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  • 13. Congenital bilateral fibular deficiency with facial dysmorphia, brachydactyly and mental retardation in a girl.
    Stoll C, Alembik Y, Repetto M.
    Genet Couns; 1998 Dec; 9(2):147-52. PubMed ID: 9664212
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  • 17. Weyers' ulnar ray/oligodactyly syndrome and the association of midline malformations with ulnar ray defects.
    Turnpenny PD, Dean JC, Duffty P, Reid JA, Carter P.
    J Med Genet; 1992 Sep; 29(9):659-62. PubMed ID: 1404297
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  • 18. 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 Sep; 14(5):310-2. PubMed ID: 10529577
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  • 20. [Prenatal diagnosis of pulmonary hypoplasia camptodactyly syndrome. Hypothesis concerning the origin of hydramnios].
    Lopes P, Talmant C, Cohen JY, Mouzard A, Nomballais MF, Boiffard JP, Lerat MF.
    J Genet Hum; 1985 Sep; 33(3-4):347-55. PubMed ID: 3903053
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