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Journal Abstract Search

135 related items for PubMed ID: 5517966

  • 1. Retinitis pigmentosa with mental retardation, deafness and XX-XO sex chromosomes.
    Jancar J.
    J Ment Defic Res; 1970 Dec; 14(4):269-73. PubMed ID: 5517966
    [No Abstract] [Full Text] [Related]

  • 2. [Usher syndrome and possible heredity linked to X chromosome].
    Baldellou Vázquez A, Navarro Zapata C, Albalad Cebrian E, Mateo Blanco A.
    An Esp Pediatr; 1993 Nov; 39(5):462-4. PubMed ID: 8285470
    [No Abstract] [Full Text] [Related]

  • 3. Seven hereditary syndromes with pigmentary retinopathy. A review and differential diagnosis.
    Cantani A, Bellioni P, Bamonte G, Salvinelli F, Bamonte MT.
    Clin Pediatr (Phila); 1985 Oct; 24(10):578-83. PubMed ID: 3896611
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  • 4. Prepubertal XX male with profound physical and mental deficiency, retinitis pigmentosa and multiple congenital anomalies.
    Pescia G, Spahr A, Genton N, Juillard E.
    Helv Paediatr Acta; 1978 Apr; 33(1):63-72. PubMed ID: 566736
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  • 5. [Retinal degeneration and deafness].
    Paufique L, Ravault MP, Morgon A.
    Confin Neurol; 1965 Apr; 25(4):318-25. PubMed ID: 5862475
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  • 10. Familial hemiplegic migraine, retinal degeneration, deafness, and nystagmus.
    Young GF, Leon-Barth CA, Green J.
    Arch Neurol; 1970 Sep; 23(3):201-9. PubMed ID: 5311627
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  • 13. [Nosology of Von Graefe-Lindenov syndrome. Study of mental disorders in this genetic neurosensory disease].
    Nehlil J.
    Ann Med Psychol (Paris); 1981 Mar; 139(3):352-6. PubMed ID: 7325492
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  • 16. Giant retinal tear in Usher syndrome type II: coincidence or association?
    Cahill MT, Barry PJ, Kenna PF.
    Retina; 1998 Mar; 18(2):177-8. PubMed ID: 9564703
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  • 18. Gross chromosomal errors in tall men admitted to mental hospitals.
    Akesson HO, Forssman H, Wallin L.
    Acta Psychiatr Scand; 1969 Mar; 45(1):37-46. PubMed ID: 5345564
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