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Journal Abstract Search

305 related items for PubMed ID: 317787

  • 1.
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  • 2. Pathologic findings in the Wolf-Hirschhorn (4p-) syndrome.
    Gonzalez CH, Capelozzi VL, Wajntal A.
    Am J Med Genet; 1981; 9(3):183-7. PubMed ID: 7282779
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  • 4. Wolf-Hirschhorn syndrome owing to 1:3 segregation of a maternal 4;21 translocation.
    Bauer K, Howard-Peebles PN, Keele D, Friedman JM.
    Am J Med Genet; 1985 Jun; 21(2):351-6. PubMed ID: 4014316
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  • 5. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat.
    Qumsiyeh MB, Stevens CA.
    Am J Med Genet; 1993 Sep 01; 47(3):387-91. PubMed ID: 8135287
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  • 6. Autosomal syndromes.
    Summitt RL.
    Pediatr Ann; 1978 Jun 01; 7(6):94-5, 97-100, 102-7 passim. PubMed ID: 149945
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  • 7. Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals: clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndrome.
    Wheeler PG, Weaver DD, Palmer CG.
    Am J Med Genet; 1995 Feb 13; 55(4):462-5. PubMed ID: 7762587
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  • 10. [Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18].
    Vivarelli R, Paolieri M, Anichini C, Scarinci R, Berardi R, Rosaia L, Pucci L.
    Boll Soc Ital Biol Sper; 1992 Apr 13; 68(4):263-9. PubMed ID: 1463601
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  • 11. Terminal deletion of chromosome 4p (4p16.3) shows a breakpoint between loci linked to Huntington disease.
    Ikonen E, Salo A, Somer M, Somer H, Pääkkönen L, Peltonen L.
    Am J Med Genet; 1992 Jul 01; 43(4):753-8. PubMed ID: 1535752
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  • 13. Elucidation of the cytogenetic abnormality in a 4p- "phenocopy".
    Curry CJ, Ying KL, O'Lague P, Tsai J.
    Birth Defects Orig Artic Ser; 1982 Jul 01; 18(3B):275-86. PubMed ID: 7139110
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  • 14. Wolf-Hirschhorn syndrome with cryptic 4p16.3 deletion and balanced/unbalanced mosaicism in the mother.
    Fryns JP, Smeets E, Devriendt K, Petit P.
    Ann Genet; 1998 Jul 01; 41(2):73-6. PubMed ID: 9706336
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  • 15. Syndromes associated with deletion of the long arm of chromosome 18[del(18q)].
    Wilson MG, Towner JW, Forsman I, Siris E.
    Am J Med Genet; 1979 Jul 01; 3(2):155-74. PubMed ID: 474629
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  • 16. [9p trisomy syndrome. Two new cases (author's transl)].
    Martín Sánchez A, Delicado A, Izquierdo M, Oliver A, López Pajares I, Gracia R, Peralta A.
    An Esp Pediatr; 1981 May 01; 14(5):344-51. PubMed ID: 7294523
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  • 17. Partial 9p monosomy in a girl with a tdic(9p23;13p11) translocation, minor anomalies, obesity, and mental retardation.
    Serra A, Bova R, Bellanova G, Chindemi A, Zappata S, Brahe C.
    Am J Med Genet; 1997 Aug 08; 71(2):139-43. PubMed ID: 9217211
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  • 18. Interstitial deletion of distal chromosome 4p in a patient without classical Wolf-Hirschhorn syndrome.
    Estabrooks LL, Rao KW, Korf B.
    Am J Med Genet; 1993 Jan 01; 45(1):97-100. PubMed ID: 8418669
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  • 20. Mild phenotype due to inverse duplication 4p16.3 - P15.3 including the Wolf-Hirschhorn critical region.
    Tschernigg M, Petek E, Wagner K, Kroisel PM.
    Genet Couns; 2002 Jan 01; 13(1):29-33. PubMed ID: 12017235
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