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PUBMED FOR HANDHELDS

Journal Abstract Search


129 related items for PubMed ID: 2624273

  • 21. Knobloch syndrome in a large Brazilian consanguineous family: confirmation of autosomal recessive inheritance.
    Passos-Bueno MR, Marie SK, Monteiro M, Neustein I, Whittle MR, Vainzof M, Zatz M.
    Am J Med Genet; 1994 Aug 15; 52(2):170-3. PubMed ID: 7802003
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  • 23. Familial congenital diaphragmatic defects: aspects of etiology, prenatal diagnosis, and treatment.
    Norio R, Kääriäinen H, Rapola J, Herva R, Kekomäki M.
    Am J Med Genet; 1984 Feb 15; 17(2):471-83. PubMed ID: 6702899
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  • 26. A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene.
    Bitner-Glindzicz M, Lindley KJ, Rutland P, Blaydon D, Smith VV, Milla PJ, Hussain K, Furth-Lavi J, Cosgrove KE, Shepherd RM, Barnes PD, O'Brien RE, Farndon PA, Sowden J, Liu XZ, Scanlan MJ, Malcolm S, Dunne MJ, Aynsley-Green A, Glaser B.
    Nat Genet; 2000 Sep 15; 26(1):56-60. PubMed ID: 10973248
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  • 32. Brief clinical report: autosomal recessive anophthalmia with multiple congenital abnormalities--type Waardenburg.
    Richieri-Costa A, Gollop TR, Otto PG.
    Am J Med Genet; 1983 Apr 15; 14(4):607-15. PubMed ID: 6846395
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  • 34. Nesidioblastosis: evidence for autosomal recessive inheritance.
    Woolf DA, Leonard JV, Trembath RC, Pembrey ME, Grant DB.
    Arch Dis Child; 1991 Apr 15; 66(4):529-30. PubMed ID: 2031615
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  • 35. Beta cell nesidioblastosis in idiopathic hypoglycemia of infancy.
    Yakovac WC, Baker L, Hummeler K.
    J Pediatr; 1971 Aug 15; 79(2):226-31. PubMed ID: 4104455
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  • 36. Familial nesidioblastosis: severe neonatal hypoglycemia in two families.
    Schwartz SS, Rich BH, Lucky AW, Straus FH, Gonen B, Wolfsdorf J, Thorp FW, Burrington JD, Madden JD, Rubenstein AH, Rosenfield RL.
    J Pediatr; 1979 Jul 15; 95(1):44-53. PubMed ID: 383929
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  • 38. Familial truncus arteriosus: a possible autosomal-recessive trait.
    Abushaban L, Uthaman B, Kumar AR, Selvan J.
    Pediatr Cardiol; 2003 Jul 15; 24(1):64-6. PubMed ID: 12574981
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  • 40. Nesidioblastosis and persistent neonatal hyperinsulinism.
    Sempoux C, Poggi F, Brunelle F, Saudubray JM, Fekete C, Rahier J.
    Diabete Metab; 1995 Dec 15; 21(6):402-7. PubMed ID: 8593920
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