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Journal Abstract Search

158 related items for PubMed ID: 2407847

  • 1. Holoprosencephaly and polydactyly: a possible expression of the hydrolethalus syndrome.
    Bachman H, Clark RD, Salahi W.
    J Med Genet; 1990 Jan; 27(1):50-2. PubMed ID: 2407847
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  • 4. [Holoprosencephaly, polydactyly, cardiopathy: new syndrome or a new case of hydrolethalus?].
    André SA, Cordier MP, Beaufrère AM, Guillaud M, Robert JM.
    J Genet Hum; 1988 Dec; 36(5):463-8. PubMed ID: 3216192
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  • 5. Familial holoprosencephaly, heart defects, and polydactyly.
    Hennekam RC, van Noort G, de la Fuente AA.
    Am J Med Genet; 1991 Nov 01; 41(2):258-62. PubMed ID: 1785646
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  • 6. Holoprosencephaly, polydactyly and normal chromosomes: pseudo-trisomy 13?
    Hewitt BG, Seller MJ, Bennett CP, Maxwell DM.
    Clin Genet; 1989 Aug 01; 36(2):141-3. PubMed ID: 2766571
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  • 7. Unknown syndrome: holoprosencephaly, congenital heart defects, and polydactyly.
    Young ID, Madders DJ.
    J Med Genet; 1987 Nov 01; 24(11):714-5. PubMed ID: 3430550
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  • 10. Holoprosencephaly and postaxial polydactyly with normal chromosomes. Another observation of a new malformation syndrome; a case report.
    Ramaekers PR, Legius E, Verloes A, Gillerot Y, Vandenberghe K, Fryns JP.
    Eur J Obstet Gynecol Reprod Biol; 1990 Nov 01; 36(1-2):161-5. PubMed ID: 2365121
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  • 11. Hydrolethalus syndrome in consecutive African siblings.
    Adetoro OO, Komolafe F, Anjorin A.
    Pediatr Radiol; 1984 Nov 01; 14(6):422-4. PubMed ID: 6390321
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  • 15. [Prenatal diagnosis of holoprosencephaly with postaxial polydactyly, cardiopathy with normal karyotype].
    Salamanca A, Padilla MC, Sabatel RM, Motos MA, Stemper K, Gonzalez-Gomez F.
    Geburtshilfe Frauenheilkd; 1992 Dec 01; 52(12):783-5. PubMed ID: 1490560
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  • 16. Hydrolethalus (Salonen-Herva-Norio) syndrome: further clinicopathological delineation.
    Anyane-Yeboa K, Collins M, Kupsky W, Maidman J, Malin J, Yeh M.
    Am J Med Genet; 1987 Apr 01; 26(4):899-907. PubMed ID: 3296755
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  • 18. Pseudo-trisomy 13 syndrome.
    Cohen MM, Gorlin RJ.
    Am J Med Genet; 1991 Jun 01; 39(3):332-5; discussion 336-7. PubMed ID: 1867286
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  • 20. A new case of holoprosencephaly-polydactyly syndrome with alobar holoprosencephaly, preaxial polydactyly and congenital glaucoma.
    Sandal G, Tok L, Ormeci AR.
    Genet Couns; 2014 Jun 01; 25(1):49-52. PubMed ID: 24783655
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