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PUBMED FOR HANDHELDS

Journal Abstract Search

195 related items for PubMed ID: 6686259

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  • 4. New syndrome: mixed hearing loss, mental deficiency, growth retardation, short clubbed digits, and EEG abnormalities in monozygous female twins.
    Pfeiffer RA.
    Am J Med Genet; 1987 Jul; 27(3):639-44. PubMed ID: 3631135
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  • 5. Orofaciodigital syndrome type IV: report of a patient.
    Nevin NC, Thomas PS.
    Am J Med Genet; 1989 Feb; 32(2):151-4. PubMed ID: 2929654
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  • 6. 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(2):119-22. PubMed ID: 7381865
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  • 13. Twin fetuses with abnormalities that overlap with three midline malformation complexes.
    Hingorani SR, Pagon RA, Shepard TH, Kapur RP.
    Am J Med Genet; 1991 Nov 01; 41(2):230-5. PubMed ID: 1785640
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  • 16. Further observations on a pedigree of the oral-facial-digital syndrome.
    Kernohan DC, Dodge JA.
    Arch Dis Child; 1969 Dec 01; 44(238):729-31. PubMed ID: 5356980
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  • 17. Oral-facial-digital syndrome with Y-shaped fourth metacarpals and endocardial cushion defect.
    Hsieh YC, Hou JW.
    Am J Med Genet; 1999 Sep 17; 86(3):278-81. PubMed ID: 10482880
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  • 18. Oro-facial-digital syndrome II. Transitional type between the Mohr and the Majewski syndromes: report of two new cases.
    Silengo MC, Bell GL, Biagioli M, Franceschini P.
    Clin Genet; 1987 May 17; 31(5):331-6. PubMed ID: 3608220
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  • 19. Jeune syndrome with tongue lobulation and preaxial polydactyly, and Jeune syndrome with situs inversus and asplenia: compound heterozygosity Jeune-Mohr and Jeune-Ivemark?
    Majewski E, Oztürk B, Gillessen-Kaesbach G.
    Am J Med Genet; 1996 May 03; 63(1):74-9. PubMed ID: 8723090
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  • 20. Long-term follow-up of a girl with oro-facio-digital syndrome type I due to a mutation in the OFD 1 gene.
    Stoll C, Sauvage P.
    Ann Genet; 2002 May 03; 45(2):59-62. PubMed ID: 12119212
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