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Journal Abstract Search

301 related items for PubMed ID: 4927796

  • 1. Hereditary congenital severe deafness syndromes.
    Konigsmark BW.
    Ann Otol Rhinol Laryngol; 1971 Apr; 80(2):269-88. PubMed ID: 4927796
    [No Abstract] [Full Text] [Related]

  • 2. [A Swiss family with Klein-Waardenburg's syndrome associated with hyperkeratosis of the palms and feet and with serious oligophrenia].
    Amini-Elihou S.
    J Genet Hum; 1970 Dec; 18(4):307-63. PubMed ID: 5524816
    [No Abstract] [Full Text] [Related]

  • 3. A coloured family showing features of Waardenburg's syndrome.
    Rappoport AS.
    S Afr Med J; 1970 Apr 04; 44(14):412-3. PubMed ID: 5443890
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  • 6. The causes of profound deafness in childhood. In: Sensorinerual hearing loss.
    Fraser GR.
    Ciba Found Symp; 1970 Apr 04; ():5-40. PubMed ID: 5210930
    [No Abstract] [Full Text] [Related]

  • 7. [Hearing disorders in Waardenburg's syndrome].
    Schulze W, Ganz H.
    HNO; 1972 Jul 04; 20(7):203-7. PubMed ID: 5071320
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  • 8. Waardenburg's syndrome with bilateral cleft lip.
    Giacoia JP, Klein SW.
    Am J Dis Child; 1969 Mar 04; 117(3):344-8. PubMed ID: 5765156
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  • 10. Heterogeneity in Waardenburg's syndrome. Report of a family with ocular albinism.
    Bard LA.
    Arch Ophthalmol; 1978 Jul 04; 96(7):1193-8. PubMed ID: 666627
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  • 15. Waardenburg's syndrome.
    Fanaroff AA, Levin SE.
    J Pediatr; 1968 Jul 04; 73(1):151. PubMed ID: 5658623
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  • 16. Waardenburg's syndrome and familial periodic paralysis.
    Tay CH.
    Postgrad Med J; 1971 Jun 04; 47(548):354-60. PubMed ID: 5580938
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  • 19. Tibial hemimelia: report on 37 new cases, clinical and genetic considerations.
    Richieri-Costa A, Ferrareto I, Masiero D, da Silva CR.
    Am J Med Genet; 1987 Aug 04; 27(4):867-84. PubMed ID: 3425598
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