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Journal Abstract Search

119 related items for PubMed ID: 4064363

  • 1. Cortical blindness, growth and psychomotor retardation and postaxial polydactyly: a probably distinct autosomal recessive syndrome.
    Hernández A, García-Esquivel L, Reynoso MC, Fragoso R, Enríquez-Guerra MA, Nazará Z, Anzar MB, Cantú JM.
    Clin Genet; 1985 Sep; 28(3):251-4. PubMed ID: 4064363
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  • 6. Kenny-Caffey syndrome in six Bedouin sibships: autosomal recessive inheritance is confirmed.
    Tahseen K, Khan S, Uma R, Usha R, Al Ghanem MM, Al Awadi SA, Farag TI.
    Am J Med Genet; 1997 Mar 17; 69(2):126-32. PubMed ID: 9056548
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  • 7. The acrocallosal syndrome.
    Philip N, Apicella N, Lassman I, Ayme S, Mattei JF, Giraud F.
    Eur J Pediatr; 1988 Feb 17; 147(2):206-8. PubMed ID: 3366141
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  • 8. Polydactyly, postaxial, type B.
    Holmes LB, Nasri H, Hunt AT, Toufaily MH, Westgate MN.
    Birth Defects Res; 2018 Jan 17; 110(2):134-141. PubMed ID: 29377639
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  • 10. Syndrome of polydactyly, cleft lip/palate or lingual lump, and psychomotor retardation in endogamic gypsies.
    Váradi V, Szabó L, Papp Z.
    J Med Genet; 1980 Apr 17; 17(2):119-22. PubMed ID: 7381865
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  • 13. Microcephaly and congenital nephrotic syndrome owing to diffuse mesangial sclerosis: an autosomal recessive syndrome.
    Garty BZ, Eisenstein B, Sandbank J, Kaffe S, Dagan R, Gadoth N.
    J Med Genet; 1994 Feb 17; 31(2):121-5. PubMed ID: 8182716
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  • 14. Probable new syndrome in a Mexican family with congenital palmar polyonychia and postaxial limb defects.
    Román Corona-Rivera J, Corona-Rivera E, Fragoso-Herrera R, Nuño-Arana I, Loera-Castañeda V.
    Am J Med Genet A; 2004 Mar 01; 125A(2):205-9. PubMed ID: 14981725
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  • 18. Brief clinical report: autosomal recessive anophthalmia with multiple congenital abnormalities--type Waardenburg.
    Richieri-Costa A, Gollop TR, Otto PG.
    Am J Med Genet; 1983 Apr 01; 14(4):607-15. PubMed ID: 6846395
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  • 19. An autosomal dominant syndrome of short stature with mesomelic shortness of limbs, abnormal carpal and tarsal bones, hypoplastic middle phalanges, and bipartite calcanei.
    Osebold WR, Remondini DJ, Lester EL, Spranger JW, Opitz JM.
    Am J Med Genet; 1985 Dec 01; 22(4):791-809. PubMed ID: 4073128
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