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Journal Abstract Search

278 related items for PubMed ID: 8741931

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  • 5. Three-generation dominant transmission of the Silver-Russell syndrome.
    Duncan PA, Hall JG, Shapiro LR, Vibert BK.
    Am J Med Genet; 1990 Feb; 35(2):245-50. PubMed ID: 2178417
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  • 8. Child with Sotos phenotype and a 5:15 translocation.
    Maroun C, Schmerler S, Hutcheon RG.
    Am J Med Genet; 1994 Apr 15; 50(3):291-3. PubMed ID: 8042674
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  • 9. Two male sibs with a previously unrecognized syndrome: facial dysmorphia, hyperextensibility of joints, clinodactyly, growth retardation and mental retardation.
    Morillo-Cucci G, Passarge E, Simpson JL, Chaganti RS, German J.
    Birth Defects Orig Artic Ser; 1975 Apr 15; 11(2):380-3. PubMed ID: 1227554
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  • 11. Guadalajara camptodactyly syndrome. A distinct probably autosomal recessive disorder.
    Cantú JM, Rivera H, Nazará Z, Rojas Q, Hernández A, García-Cruz D.
    Clin Genet; 1980 Sep 15; 18(3):153-9. PubMed ID: 7192193
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  • 14. An autosomal dominant syndrome of characteristic facial appearance, preauricular pits, fifth finger clinodactyly, and tetralogy of Fallot.
    Jones MC, Waldman JD.
    Am J Med Genet; 1985 Sep 15; 22(1):135-41. PubMed ID: 4050848
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  • 17. Clinical and molecular findings in two patients with russell-silver syndrome and UPD7: comparison with non-UPD7 cases.
    Bernard LE, Peñaherrera MS, Van Allen MI, Wang MS, Yong SL, Gareis F, Langlois S, Robinson WP.
    Am J Med Genet; 1999 Nov 26; 87(3):230-6. PubMed ID: 10564876
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  • 18. Identification of two new polymorphisms (c2447-125A>G; c2532G>A) in the gamma 2-COP (COPG2) gene by screening of Silver-Russell syndrome patients.
    Mergenthaler S, Blagitko-Dorfs N, Wollmann HA, Ranke MB, Ropers HH, Kalscheuer VM, Eggermann T.
    Hum Mutat; 2000 Jul 26; 16(1):96. PubMed ID: 10874328
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