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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

202 related items for PubMed ID: 7258227

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  • 3. Camptodactyly, cleft palate, and club foot. A syndrome showing the autosomal-dominant pattern of inheritance.
    Gordon H, Davies D, Berman M.
    J Med Genet; 1969 Sep; 6(3):266-74. PubMed ID: 5345097
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  • 4. Dominantly inherited syndrome of microcephaly and cleft palate.
    Halal F.
    Am J Med Genet; 1983 May; 15(1):135-40. PubMed ID: 6859112
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  • 5. Scoliosis in Gordon's syndrome.
    Wild A, Schillians N, Kumar M, Mehdian SH.
    Eur Spine J; 2001 Oct; 10(5):458-60. PubMed ID: 11718203
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  • 6. Mesomelic limb shortness: a previously unreported autosomal recessive type.
    Reardon W, Hall CM, Slaney S, Huson SM, Connell J, al-Hilaly N, Fixsen J, Baraitser M, Winter RM.
    Am J Med Genet; 1993 Oct 01; 47(5):788-92. PubMed ID: 8267013
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  • 8. Genitourinary anomalies are a component manifestation in the ectodermal dysplasia, ectrodactyly, cleft lip/palate (EEC) syndrome.
    Rollnick BR, Hoo JJ.
    Am J Med Genet; 1988 Jan 01; 29(1):131-6. PubMed ID: 3278611
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  • 12. Schilbach-Rott syndrome in a third family: further delineation of an autosomal dominant trait.
    Becerra-Solano LE, Casillas-Avila MP, Díaz-Rodríguez M, Nastasi-Catanese JA, Toscano-Flores JJ, Ramírez-Dueñas ML.
    Genet Couns; 2007 Jan 01; 18(3):317-23. PubMed ID: 18019373
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  • 13. New syndrome in three affected siblings.
    Crane JP, Heise RL.
    Pediatrics; 1981 Aug 01; 68(2):235-7. PubMed ID: 7267231
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  • 14. Dominant inheritance of cleft palate with minor abnormalities of hands and feet: a new syndrome?
    Kirk EP, Wilson M.
    Clin Dysmorphol; 1999 Jul 01; 8(3):193-7. PubMed ID: 10457853
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  • 15. Short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot: a new autosomal recessive syndrome.
    Richieri-Costa A, Pereira SC.
    Am J Med Genet; 1992 Mar 01; 42(5):681-7. PubMed ID: 1632438
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  • 16. Robin sequence and oligodactyly in mother and son.
    Robinow M, Johnson GF, Apesos J.
    Am J Med Genet; 1986 Oct 01; 25(2):293-7. PubMed ID: 3777025
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  • 17. Phenotypic overlap of the BBB and G syndromes.
    Cordero JF, Holmes LB.
    Am J Med Genet; 1978 Oct 01; 2(2):145-52. PubMed ID: 263434
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  • 18. Syndactyly type V.
    Robinow M, Johnson GF, Broock GJ.
    Am J Med Genet; 1982 Apr 01; 11(4):475-82. PubMed ID: 6283889
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  • 19. 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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  • 20. A familial syndrome with micrognathia, cleft palate, short neck and stature, vertebral anomalies and mental retardation.
    Mathieu M, De Broca A, Bony H, Piussan C.
    Genet Couns; 1993 Nov 06; 4(4):299-303. PubMed ID: 8110419
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