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PUBMED FOR HANDHELDS

Journal Abstract Search

176 related items for PubMed ID: 3717209

  • 1.
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  • 2. The distal arthrogryposes: delineation of new entities--review and nosologic discussion.
    Hall JG, Reed SD, Greene G.
    Am J Med Genet; 1982 Feb; 11(2):185-239. PubMed ID: 7039311
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  • 4. Limb pterygium syndromes: a review and report of eleven patients.
    Hall JG, Reed SD, Rosenbaum KN, Gershanik J, Chen H, Wilson KM.
    Am J Med Genet; 1982 Aug; 12(4):377-409. PubMed ID: 7124793
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  • 5. Ovine heritable arthrogryposis multiplex congenita with probable lethal autosomal recessive mutation.
    Tejedor MT, Ferrer LM, Monteagudo LV, Ramos JJ, Lacasta D, Climent S.
    J Comp Pathol; 2010 Jul; 143(1):14-9. PubMed ID: 20153865
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  • 6. Cleft palate, ptosis, digital anomalies and mental retardation: a new syndrome or a distal arthrogryposis variant?
    Boles RG.
    Clin Dysmorphol; 1999 Jan; 8(1):63-5. PubMed ID: 10327254
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  • 7. Extending the spectrum of distal arthrogryposis.
    Gripp KW, Scott CI, Brockett BC, Nicholson L, Mackenzie WG.
    Am J Med Genet; 1996 Nov 11; 65(4):286-90. PubMed ID: 8923937
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  • 8. Familial distal arthrogryposis with craniofacial abnormalities: a new subtype of type II?
    Moore CA, Weaver DD.
    Am J Med Genet; 1989 Jun 11; 33(2):231-7. PubMed ID: 2764034
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  • 10. Distinct craniofacial syndrome of lagophthalmia and bilateral cleft lip and palate.
    Korula S, Wilson L, Salomonson J.
    Am J Med Genet; 1995 Nov 06; 59(2):229-33. PubMed ID: 8588591
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  • 11. Distal arthrogryposis type IIB: further clinical delineation and 54-year follow-up of an index case.
    Friedman BD, Heidenreich RA.
    Am J Med Genet; 1995 Aug 28; 58(2):125-7. PubMed ID: 8533802
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  • 12. Familial Gordon syndrome associated with a PIEZO2 mutation.
    Alisch F, Weichert A, Kalache K, Paradiso V, Longardt AC, Dame C, Hoffmann K, Horn D.
    Am J Med Genet A; 2017 Jan 28; 173(1):254-259. PubMed ID: 27714920
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  • 17. [Heredity and empirical hereditary prognosis of cleft lip and palate in 326 cases out of 309 unselected Swiss families].
    Hanhart E, Kälin A.
    J Genet Hum; 1972 Jun 28; 20(2):93-134. PubMed ID: 4660640
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  • 18. A distinct syndrome of familial cleft lip and palate with prominent eyes and characteristic facies in two unrelated families.
    Kumar D, Garcia-Minaur S, Quarrell OW, Landa G, Garaizar C.
    Clin Dysmorphol; 1996 Oct 28; 5(4):295-301. PubMed ID: 8905193
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  • 19. An unusual distal arthrogryposis.
    Kawira EL, Bender HA.
    Am J Med Genet; 1985 Mar 28; 20(3):425-9. PubMed ID: 3993671
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  • 20. [Congenital multiple arthrogryposis. Clinical and genetic study].
    Gallegos-Rivera M, Carnevale A, Valdés H, del Castillo V.
    Bol Med Hosp Infant Mex; 1991 Feb 28; 48(2):88-95. PubMed ID: 2054091
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