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Journal Abstract Search

263 related items for PubMed ID: 6487184

  • 21. Laurence-Moon syndrome: evaluation of endocrinological function and phenotypic concordance and report of cases.
    Dekaban AS, Parks JS, Ross GT.
    Med Ann Dist Columbia; 1972 Nov; 41(11):687-94. PubMed ID: 4508225
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  • 22. Bardet-biedl syndrome and brain abnormalities.
    Rooryck C, Pelras S, Chateil JF, Cances C, Arveiler B, Verloes A, Lacombe D, Goizet C.
    Neuropediatrics; 2007 Feb; 38(1):5-9. PubMed ID: 17607597
    [Abstract] [Full Text] [Related]

  • 23. The Laurence-Moon-Bardet-Biedl-syndrome.
    Luz MF, Marques MN, Jorge E, Jacomini CZ, Ribero Z, Marques J.
    Metab Pediatr Syst Ophthalmol (1985); 1985 Feb; 8(2-3):15-20. PubMed ID: 3870940
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  • 24. Linkage of Bardet-Biedl syndrome to chromosome 16q and evidence for non-allelic genetic heterogeneity.
    Kwitek-Black AE, Carmi R, Duyk GM, Buetow KH, Elbedour K, Parvari R, Yandava CN, Stone EM, Sheffield VC.
    Nat Genet; 1993 Dec; 5(4):392-6. PubMed ID: 8298649
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  • 25. Bardet-Biedl syndrome: a case series.
    Elawad OAMA, Dafallah MA, Ahmed MMM, Albashir AAD, Abdalla SMA, Yousif HHM, Daw Elbait AAE, Mohammed ME, Ali HIH, Ahmed MMM, Mohammed NFN, Osman FHM, Mohammed MAY, Abu Shama EAE.
    J Med Case Rep; 2022 Apr 29; 16(1):169. PubMed ID: 35484558
    [Abstract] [Full Text] [Related]

  • 26. [A case of familial Bardet-Biedl syndrome (obesity, slight mental retardation, polydactyly, retinitis pigmentosum and renal failure) with insulin-resistant diabetes mellitus].
    Iannello S, Fagone S, Grasso G, Ierna D, Meli S, Pennisi P, Perrotta C, Zingali C, Belfiore F.
    Minerva Endocrinol; 1998 Sep 29; 23(3):83-92. PubMed ID: 10063326
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  • 29. Rud syndrome: congenital ichthyosis, hypogonadism, mental retardation, retinitis pigmentosa and hypertrophic polyneuropathy.
    Larbrisseau A, Carpenter S.
    Neuropediatrics; 1982 May 29; 13(2):95-8. PubMed ID: 6182503
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  • 30. [Renal involvement in the Laurence-Moon-Bardet-Biedl syndrome. Apropos of 3 cases].
    Gourdol O, David L, Colon S, Bouvier R, Ayral A, Aguercif M, François R.
    Pediatrie; 1984 May 29; 39(3):175-81. PubMed ID: 6473010
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  • 32. A Case of Laurence Moon Bardet Biedl Syndrome.
    Indraneel KS, VRajalakshmi, Dayanandan Y, Reddy NM.
    J Assoc Physicians India; 2023 Jan 29; 71(1):1. PubMed ID: 37116049
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  • 36. Bardet-Biedl syndrome is linked to DNA markers on chromosome 11q and is genetically heterogeneous.
    Leppert M, Baird L, Anderson KL, Otterud B, Lupski JR, Lewis RA.
    Nat Genet; 1994 May 29; 7(1):108-12. PubMed ID: 8075632
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  • 37. A family with the Bardet-Biedl syndrome and diabetes mellitus.
    Escallon F, Traboulsi EI, Infante R.
    Arch Ophthalmol; 1989 Jun 29; 107(6):855-7. PubMed ID: 2730406
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  • 38. Hydrometrocolpos and polydactyly: a common neonatal presentation of Bardet-Biedl and McKusick-Kaufman syndromes.
    David A, Bitoun P, Lacombe D, Lambert JC, Nivelon A, Vigneron J, Verloes A.
    J Med Genet; 1999 Aug 29; 36(8):599-603. PubMed ID: 10465109
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  • 39. [Laurence-Moon-Bardet-Biedl syndrome].
    Kränke B, Januschowski R, Balzer K.
    Med Klin (Munich); 1993 Feb 15; 88(2):78-81. PubMed ID: 8450812
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