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 *

183 related articles for article (PubMed ID: 29482283)

  • 21. [Historical development of human genetics].
    Sretenović Z
    Med Glas; 1966; 20(5):208-14. PubMed ID: 5333626
    [No Abstract]   [Full Text] [Related]  

  • 22. [Patho-physiology of renal dysfunction in Bardet-Biedl Syndrome].
    Zona E; Zacchia M; Di Iorio V; Capolongo G; Rinaldi L; Capasso G
    G Ital Nefrol; 2017 Sep; 34(5):62-72. PubMed ID: 28963828
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Choroidal neovascularization in Bardet-Biedl syndrome.
    Charkoudian LD; Barañano DE; Fortun J; Yan J; Srivastava SK
    Ophthalmic Genet; 2013; 34(1-2):52-4. PubMed ID: 23565731
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Mutation analysis of the MKKS gene in McKusick-Kaufman syndrome and selected Bardet-Biedl syndrome patients.
    Slavotinek AM; Searby C; Al-Gazali L; Hennekam RC; Schrander-Stumpel C; Orcana-Losa M; Pardo-Reoyo S; Cantani A; Kumar D; Capellini Q; Neri G; Zackai E; Biesecker LG
    Hum Genet; 2002 Jun; 110(6):561-7. PubMed ID: 12107442
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Primer on medical genomics part I: History of genetics and sequencing of the human genome.
    Lorentz CP; Wieben ED; Tefferi A; Whiteman DA; Dewald GW
    Mayo Clin Proc; 2002 Aug; 77(8):773-82. PubMed ID: 12173713
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Rheumatic valvular insufficiency in Bardet-Biedl syndrome: a case report.
    Purkait R; Roy BN; Samanta T; Mallick AK; Sinhamahapatra T
    J Indian Med Assoc; 2012 Sep; 110(9):651-2. PubMed ID: 23741841
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Progress of research on Bardet-Biedl syndrome].
    Zeng P; Shen T
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr; 35(2):288-292. PubMed ID: 29653013
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Hydrometrocolpos and acute renal failure: a rare neonatal presentation of Bardet-Biedl syndrome.
    Cherian MP; Al-Sanna'a NA; Ayyat FM
    J Pediatr Urol; 2008 Aug; 4(4):313-6. PubMed ID: 18644538
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Genetics].
    Czeizel E
    Orv Hetil; 1989 Jan; 130(4):187-9. PubMed ID: 2643791
    [No Abstract]   [Full Text] [Related]  

  • 30. [From the history of establishment of medical genetics in Russia].
    Bochkov NP; Filippova MG; Stochik AM; Zatravkin SN; Makarova OA
    Vestn Ross Akad Med Nauk; 2000; (7):51-3. PubMed ID: 10961151
    [No Abstract]   [Full Text] [Related]  

  • 31. Targeted multi-gene panel testing for the diagnosis of Bardet Biedl syndrome: Identification of nine novel mutations across BBS1, BBS2, BBS4, BBS7, BBS9, BBS10 genes.
    Ece Solmaz A; Onay H; Atik T; Aykut A; Cerrah Gunes M; Ozalp Yuregir O; Bas VN; Hazan F; Kirbiyik O; Ozkinay F
    Eur J Med Genet; 2015 Dec; 58(12):689-94. PubMed ID: 26518167
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Polydactyly and obesity - the clinical manifestation of ciliopathy: a boy with Bardet-Biedl syndrome.
    Szmigielska A; Krzemień G; Roszkowska-Blaim M; Obersztyn E
    Dev Period Med; 2016; 20(2):105-9. PubMed ID: 27442694
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 34. On the origin of genetics and beginnings of medical genetics of diseases of the kidney.
    Eknoyan G
    Adv Chronic Kidney Dis; 2006 Apr; 13(2):174-7. PubMed ID: 16580619
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Contradictions in the history of genetics].
    Czeizel E
    Orv Hetil; 1982 Feb; 123(6):349-57. PubMed ID: 7043363
    [No Abstract]   [Full Text] [Related]  

  • 36. Asymptomatic renal cell carcinoma as a finding of Bardet Biedl syndrome.
    Zaldivar RA; Neale MD; Evans WE; Pulido JS
    Ophthalmic Genet; 2008 Mar; 29(1):33-5. PubMed ID: 18363171
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Clinical characteristics of a Japanese patient with Bardet-Biedl syndrome caused by BBS10 mutations.
    Kurata K; Hosono K; Hikoya A; Kato A; Saitsu H; Minoshima S; Ogata T; Hotta Y
    Jpn J Ophthalmol; 2018 Jul; 62(4):458-466. PubMed ID: 29666954
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [History of clinical genetics in psychiatry].
    Shevchenko VV
    Vrach Delo; 1974 Oct; 0(10):118-20. PubMed ID: 4609248
    [No Abstract]   [Full Text] [Related]  

  • 39. Use of isolated populations in the study of a human obesity syndrome, the Bardet-Biedl syndrome.
    Sheffield VC
    Pediatr Res; 2004 Jun; 55(6):908-11. PubMed ID: 15155861
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Bardet-Biedl syndrome associated with glaucoma.
    Ventura MP; Vianna RN; Solari HP; Filho JP; Burnier MN
    Eye (Lond); 2006 Jan; 20(1):114-6. PubMed ID: 15746958
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.