These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 2773984)

  • 1. Lethal form of fibuloulnar A/hypoplasia with renal abnormalities.
    Saito N; Kuba A; Tsuruta T
    Am J Med Genet; 1989 Apr; 32(4):452-6. PubMed ID: 2773984
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [Lethal mandibulofacial and ulnofibular dysostosis].
    Poissonnier M; Neuville V; Petit P; Busuttil R
    Ann Pediatr (Paris); 1983 Nov; 30(9):713-7. PubMed ID: 6686424
    [No Abstract]   [Full Text] [Related]  

  • 4. Femur- fibula- ulna complex.
    Geniets C; Vanhoenacker F; Blaumeiser B; Parizel PM
    JBR-BTR; 2006; 89(3):130-1. PubMed ID: 16883757
    [No Abstract]   [Full Text] [Related]  

  • 5. [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]  

  • 6. A "new" lethal multiple congenital anomaly syndrome: joint contractures, cerebellar hypoplasia, renal hypoplasia, urogenital anomalies, tongue cysts, shortness of limbs, eye abnormalities, defects of the heart, gallbladder agenesis, and ear malformations.
    Rutledge JC; Friedman JM; Harrod MJ; Currarino G; Wright CG; Pinckney L; Chen H
    Am J Med Genet; 1984 Oct; 19(2):255-64. PubMed ID: 6507477
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Miller postaxial acrofacial dysostosis syndrome. Follow-up data of a family and confirmation of autosomal recessive inheritance.
    Chrzanowska K; Fryns JP
    Clin Genet; 1993 May; 43(5):270. PubMed ID: 8375109
    [No Abstract]   [Full Text] [Related]  

  • 9. 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]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndrome.
    Chen H; Immken L; Lachman R; Yang S; Rimoin DL; Rightmire D; Eteson D; Stewart F; Beemer FA; Opitz JM
    Am J Med Genet; 1984 Apr; 17(4):809-26. PubMed ID: 6720746
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Prenatal diagnosis of femur-fibula-ulna complex by ultrasound examination at 20 weeks of gestation.
    Geipel A; Berg C; Germer U; Krokowski M; Smrcek J; Gembruch U
    Ultrasound Obstet Gynecol; 2003 Jul; 22(1):79-81. PubMed ID: 12858309
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A new syndrome of microtia with mixed type hearing loss, renal agenesis, and multiple skeletal anomalies.
    Demir Y; Samli H; Yucel A; Yilmaz MD; Haktanir NT; Maralcan G; Solak M
    Am J Med Genet A; 2006 Apr; 140(7):747-51. PubMed ID: 16502432
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fibular a/hypoplasia: review and documentation of the fibular developmental field.
    Lewin SO; Opitz JM
    Am J Med Genet Suppl; 1986; 2():215-38. PubMed ID: 3146293
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Humero-radial synostosis with ulnar defects in sibs.
    Ramer JC; Ladda RL
    Am J Med Genet; 1989 Jun; 33(2):176-9. PubMed ID: 2669480
    [TBL] [Abstract][Full Text] [Related]  

  • 16. De novo 21q interstitial deletion in a retarded boy with ulno-fibular dysostosis.
    Reynolds JF; Wyandt HE; Kelly TE
    Am J Med Genet; 1985 Jan; 20(1):173-80. PubMed ID: 3970070
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Spondylothoracic dysostosis associated with diaphragmatic hernia and camptodactyly.
    Swietliński J; Swist-Szulik K; Maruniak-Chudek I; Pyrkosz A
    Genet Couns; 2002; 13(3):309-17. PubMed ID: 12416639
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Tibial/femoral hypoplasia with "hook" pelvis: a potentially unique dysostosis.
    Mégarbané A; Ghanem I
    Am J Med Genet; 2002 Nov; 112(4):394-6. PubMed ID: 12376943
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Child with manifestations of Nager acrofacial dysostosis, and the MURCS, VACTERL, and pulmonary agenesis associations: complex defect of blastogenesis?
    David A; Mercier J; Verloes A
    Am J Med Genet; 1996 Mar; 62(1):1-5. PubMed ID: 8779315
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.