These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

217 related articles for article (PubMed ID: 7987310)

  • 41. [Bardet-Biedl syndrome. Apropos of a family].
    Guízar-Vázquez JJ; Escobar-Morales BG; Valdés de Fromow ML; Salamanca-Gómez F
    Bol Med Hosp Infant Mex; 1984 Aug; 41(8):442-6. PubMed ID: 6477712
    [No Abstract]   [Full Text] [Related]  

  • 42. Laurence Moon Bardet Biedl Syndrome.
    Abdulla AB; Niloy AA; Shah TA; Biswas SK; Imran AK; Murshed KM; Ahmed M
    Mymensingh Med J; 2009 Jan; 18(1 Suppl):S124-128. PubMed ID: 19377420
    [TBL] [Abstract][Full Text] [Related]  

  • 43. [Two sisters with Laurence Bardet-Biedl-Moon syndrome and concomittant carcinoma of the body of the uterus (author's transl)].
    Schwab G; Kriz K
    Geburtshilfe Frauenheilkd; 1980 Mar; 40(3):279-81. PubMed ID: 7364192
    [TBL] [Abstract][Full Text] [Related]  

  • 44. The Laurence-Moon-Bardet-Biedl-syndrome.
    Luz MF; Marques MN; Jorge E; Jacomini CZ; Ribero Z; Marques J
    Metab Pediatr Syst Ophthalmol (1985); 1985; 8(2-3):15-20. PubMed ID: 3870940
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Bardet-Biedl syndrome and retinitis punctata albescens in an isolated northern Canadian community.
    Pearce WG; Gillan JG; Brosseau L
    Can J Ophthalmol; 1984 Apr; 19(3):115-8. PubMed ID: 6733577
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Laurence-Moon-Bardet-Biedl Syndrome with Coexisting Abdominal Distension and Positive Fluid Thrill: A Rare Manifestation Reported in Karachi, Pakistan.
    Qadar LT; Ahmed ZM; Munawar M; Hasan CA; Iqbal SU
    Cureus; 2019 Jun; 11(6):e4885. PubMed ID: 31497414
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [The Laurence-Moon Bardet-Biedl syndrome (Casuistic contribution)].
    PALESI S; SANTOPADRE I
    Clin Pediatr (Bologna); 1959 Nov; 41():887-911. PubMed ID: 14429905
    [No Abstract]   [Full Text] [Related]  

  • 48. Bardet-Biedl syndrome.
    Keith CG
    Aust J Ophthalmol; 1984 May; 12(2):143-8. PubMed ID: 6487184
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Bardet-Biedl Syndrome: A Rare Case From Ophthalmology Perspective.
    Alhamoud M; Alnosair G; Alhashim H
    Cureus; 2022 Oct; 14(10):e29912. PubMed ID: 36348931
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Renal transplantation in patients with Bardet-Biedl syndrome.
    Sharifian M; Dadkhah-Chimeh M; Einollahi B; Nafar M; Simforoush N; Basiri A; Otukesh H
    Arch Iran Med; 2007 Jul; 10(3):339-42. PubMed ID: 17604471
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Polydactyly and hypertension.
    Isik D; Bulut O; Sunay M; Bekerecioglu M
    Ann Plast Surg; 2008 Nov; 61(5):511-2. PubMed ID: 18948777
    [TBL] [Abstract][Full Text] [Related]  

  • 52. [The value of echography in the early diagnosis of renal lesions in the Laurence-Moon-Bardet-Biedl syndrome. Apropos of a case].
    Colin D; Meunier P; Forestier D; Le Fur JM; Le Guyader J; Bellet M
    J Radiol; 1989 Jan; 70(1):61-4. PubMed ID: 2654380
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Evaluation and molecular characterization of EHD1, a candidate gene for Bardet-Biedl syndrome 1 (BBS1).
    Haider NB; Searby C; Galperin E; Mintz L; Horowitz M; Stone EM; Sheffield VC
    Gene; 1999 Nov; 240(1):227-32. PubMed ID: 10564830
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Bardet-Biedl syndrome with syndrome X: a patient report.
    Keskin M; Atabek ME; Kurtoğlu S
    J Pediatr Endocrinol Metab; 2004 Jun; 17(6):913-5. PubMed ID: 15270411
    [TBL] [Abstract][Full Text] [Related]  

  • 55. MORM syndrome (mental retardation, truncal obesity, retinal dystrophy and micropenis), a new autosomal recessive disorder, links to 9q34.
    Hampshire DJ; Ayub M; Springell K; Roberts E; Jafri H; Rashid Y; Bond J; Riley JH; Woods CG
    Eur J Hum Genet; 2006 May; 14(5):543-8. PubMed ID: 16493448
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Identification of 11 novel mutations in eight BBS genes by high-resolution homozygosity mapping.
    Harville HM; Held S; Diaz-Font A; Davis EE; Diplas BH; Lewis RA; Borochowitz ZU; Zhou W; Chaki M; MacDonald J; Kayserili H; Beales PL; Katsanis N; Otto E; Hildebrandt F
    J Med Genet; 2010 Apr; 47(4):262-7. PubMed ID: 19797195
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Cerebellar vermis hypoplasia in a patient with Bardet-Biedl syndrome.
    Baskin E; Kayiran SM; Oto S; Alehan F; Agildere AM; Saatçi U
    J Child Neurol; 2002 May; 17(5):385-7. PubMed ID: 12150587
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Laurence Moon Bardet Biedl syndrome associated with dyslipoproteinaemia.
    Desai HH; Patel M; Gonsai RN
    J Indian Med Assoc; 2011 Sep; 109(9):678. PubMed ID: 22480106
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Bardet-Biedl and Laurence-Moon syndromes in a mixed Arab population.
    Farag TI; Teebi AS
    Clin Genet; 1988 Feb; 33(2):78-82. PubMed ID: 3359670
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Bardet-Biedl syndrome and keratoconus.
    François J; Neetens A; Smets RM
    Bull Soc Belge Ophtalmol; 1982; 203():117-21. PubMed ID: 7187614
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.