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192 related items for PubMed ID: 9677055

  • 1. High incidence of autosomal recessive nonsyndromal congenital retinal nonattachment (NCRNA) in an Iranian founding population.
    Ghiasvand NM, Shirzad E, Naghavi M, Vaez Mahdavi MR.
    Am J Med Genet; 1998 Jul 07; 78(3):226-32. PubMed ID: 9677055
    [Abstract] [Full Text] [Related]

  • 2. Genetic fine mapping of the gene for nonsyndromic congenital retinal nonattachment.
    Ghiasvand NM, Fleming TP, Helms C, Avisa A, Donis-Keller H.
    Am J Med Genet; 2000 May 29; 92(3):220-3. PubMed ID: 10817658
    [Abstract] [Full Text] [Related]

  • 3. Concordance and recessive inheritance of Leber congenital amaurosis.
    Lambert SR, Sherman S, Taylor D, Kriss A, Coffey R, Pembrey M.
    Am J Med Genet; 1993 May 15; 46(3):275-7. PubMed ID: 8488871
    [Abstract] [Full Text] [Related]

  • 4. Epidemiology and genetics of primary congenital glaucoma in Slovakia. Description of a form of primary congenital glaucoma in gypsies with autosomal-recessive inheritance and complete penetrance.
    Genĉík A.
    Dev Ophthalmol; 1989 May 15; 16():76-115. PubMed ID: 2676634
    [Abstract] [Full Text] [Related]

  • 5. Congenital blindness with ocular developmental anomalies, including retinal dysplasia, in Doberman Pinscher dogs.
    Bergsjø T, Arnesen K, Heim P, Nes N.
    J Am Vet Med Assoc; 1984 Jun 01; 184(11):1383-6. PubMed ID: 6429110
    [Abstract] [Full Text] [Related]

  • 6. Genetical studies in nontraumatic retinal dialysis.
    Verdaguer TJ, Rojas B, Lechuga M.
    Mod Probl Ophthalmol; 1975 Jun 01; 15():34-9. PubMed ID: 1160913
    [Abstract] [Full Text] [Related]

  • 7. A distinct autosomal recessive ocular anomaly in Chaharborj, Islamic Republic of Iran.
    Khakshoor H, Daneshvar R, Banaee T, Tabatabaee Yazdi SA, Hasanzadeh Nazarabadi M, Moosavi M, Tavassoli F, Mahdavi R.
    East Mediterr Health J; 2012 Jan 01; 18(1):24-30. PubMed ID: 22360007
    [Abstract] [Full Text] [Related]

  • 8. Inherited retinal dysplasia and persistent hyperplastic primary vitreous in Miniature Schnauzer dogs.
    Grahn BH, Storey ES, McMillan C.
    Vet Ophthalmol; 2004 Jan 01; 7(3):151-8. PubMed ID: 15091321
    [Abstract] [Full Text] [Related]

  • 9. Juvenile cataract in Hutterites.
    Shokeir MH, Lowry RB.
    Am J Med Genet; 1985 Nov 01; 22(3):495-500. PubMed ID: 4061486
    [Abstract] [Full Text] [Related]

  • 10. Choanal atresia: evidence for autosomal recessive inheritance.
    Gershoni-Baruch R.
    Am J Med Genet; 1992 Dec 01; 44(6):754-6. PubMed ID: 1481842
    [Abstract] [Full Text] [Related]

  • 11. Nonsyndromal anencephaly: possible autosomal recessive variant.
    Farag TI, Teebi AS, Al-Awadi SA.
    Am J Med Genet; 1986 Jul 01; 24(3):461-4. PubMed ID: 3728564
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. Melnick-Needles syndrome: indication for an autosomal recessive form.
    ter Haar B, Hamel B, Hendriks J, de Jager J.
    Am J Med Genet; 1982 Dec 15; 13(4):469-77. PubMed ID: 7158646
    [Abstract] [Full Text] [Related]

  • 14. Arthrogryposis multiplex congenita in an Arab kindred: update.
    Jaber L, Weitz R, Bu X, Fischel-Ghodsian N, Rotter JI, Shohat M.
    Am J Med Genet; 1995 Jan 30; 55(3):331-4. PubMed ID: 7726232
    [Abstract] [Full Text] [Related]

  • 15. Hypoplastic left heart. Evidence for possible autosomal recessive inheritance.
    Shokeir MH.
    Birth Defects Orig Artic Ser; 1974 Jan 30; 10(4):223-7. PubMed ID: 4470892
    [Abstract] [Full Text] [Related]

  • 16. Founder effect of the 669insA mutation in BSCL2 gene causing Berardinelli-Seip congenital lipodystrophy in a cluster from Brazil.
    Gomes KB, Pardini VC, Ferreira AC, Fonseca CG, Fernandes AP.
    Ann Hum Genet; 2007 Nov 30; 71(Pt 6):729-34. PubMed ID: 17535271
    [Abstract] [Full Text] [Related]

  • 17. Epidemiological and genetic studies of congenital profound deafness in the general population of Sichuan, China.
    Liu X, Xu L, Zhang S, Xu Y.
    Am J Med Genet; 1994 Nov 01; 53(2):192-5. PubMed ID: 7856647
    [Abstract] [Full Text] [Related]

  • 18. Congenital vocal cord paralysis with possible autosomal recessive inheritance: case report and review of the literature.
    Koppel R, Friedman S, Fallet S.
    Am J Med Genet; 1996 Aug 23; 64(3):485-7. PubMed ID: 8862626
    [Abstract] [Full Text] [Related]

  • 19. Diagnostic survey at Yamanashi School for Blind: importance of heredity.
    Tsukahara S, Sasamoto M, Watanabe I, Phillips CI.
    Jpn J Ophthalmol; 1985 Aug 23; 29(3):315-21. PubMed ID: 4079129
    [Abstract] [Full Text] [Related]

  • 20. A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite Jews.
    Auslender N, Sharon D, Abbasi AH, Garzozi HJ, Banin E, Ben-Yosef T.
    Invest Ophthalmol Vis Sci; 2007 Dec 23; 48(12):5431-8. PubMed ID: 18055789
    [Abstract] [Full Text] [Related]

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