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 *

37 related articles for article (PubMed ID: 31596948)

  • 1. Second case of Bardet-Biedl syndrome caused by biallelic variants in IFT74.
    Kleinendorst L; Alsters SIM; Abawi O; Waisfisz Q; Boon EMJ; van den Akker ELT; van Haelst MM
    Eur J Hum Genet; 2020 Jul; 28(7):943-946. PubMed ID: 32144365
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Bardet Biedl syndrome: A rare genetic disorder.
    Khan SA; Ahmad Ansari MZ; Khalid M
    J Pak Med Assoc; 2020 Sep; 70(9):1651-1652. PubMed ID: 33040131
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mechanistic insights into Bardet-Biedl syndrome, a model ciliopathy.
    Zaghloul NA; Katsanis N
    J Clin Invest; 2009 Mar; 119(3):428-37. PubMed ID: 19252258
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Bardet-Biedl Syndrome-Multiple Kaleidoscope Images: Insight into Mechanisms of Genotype-Phenotype Correlations.
    Florea L; Caba L; Gorduza EV
    Genes (Basel); 2021 Aug; 12(9):. PubMed ID: 34573333
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Bardet-Biedl syndrome associated with novel compound heterozygous variants in BBS12 gene.
    Morohashi T; Hayashi T; Mizobuchi K; Nakano T; Morioka I
    Doc Ophthalmol; 2023 Apr; 146(2):165-171. PubMed ID: 36574078
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Recurrent insertional polydactyly and situs inversus in a Bardet-Biedl syndrome family.
    Deffert C; Niel F; Mochel F; Barrey C; Romana C; Souied E; Stoetzel C; Goossens M; Dollfus H; Verloes A; Girodon E; Gerard-Blanluet M
    Am J Med Genet A; 2007 Jan; 143A(2):208-13. PubMed ID: 17163542
    [No Abstract]   [Full Text] [Related]  

  • 7. Bardet-Biedl syndrome: a rare case report from North India.
    Kumar S; Mahajan BB; Mittal J
    Indian J Dermatol Venereol Leprol; 2012; 78(2):228. PubMed ID: 22421669
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mutational analysis of SDCCAG8 in Bardet-Biedl syndrome patients with renal involvement and absent polydactyly.
    Billingsley G; Vincent A; Deveault C; Héon E
    Ophthalmic Genet; 2012 Sep; 33(3):150-4. PubMed ID: 22626039
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Bardet-Biedl syndrome.
    Forsythe E; Beales PL
    Eur J Hum Genet; 2013 Jan; 21(1):8-13. PubMed ID: 22713813
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Toni Mochty: Bardet Biedl syndrome "avant la lettre".
    de Herder W
    Clin Genet; 2020 Mar; 97(3):536-537. PubMed ID: 31596948
    [No Abstract]   [Full Text] [Related]  

  • 11. Genetics of human Bardet-Biedl syndrome, an updates.
    Khan SA; Muhammad N; Khan MA; Kamal A; Rehman ZU; Khan S
    Clin Genet; 2016 Jul; 90(1):3-15. PubMed ID: 26762677
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Progress of research on the pathogenesis of obesity in Bardet-Biedl syndrome].
    Sheng H; Wang Z; Shen T
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Dec; 33(6):871-874. PubMed ID: 27984625
    [TBL] [Abstract][Full Text] [Related]  

  • 13.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 14.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 15.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 16.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 17.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 18.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 19.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 2.