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 *

129 related articles for article (PubMed ID: 21377971)

  • 1. [Mutation analysis of the pathogenic gene in a Chinese family with Brachydactyly type B1].
    Li CM; Wang FY; Sun WW; Han SL; Chang MX; Feng HG
    Yi Chuan; 2011 Feb; 33(2):147-52. PubMed ID: 21377971
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Identification of a recurrent mutation in the ROR2 gene in a Chinese family with brachydactyly type B].
    Yang W; Tan FQ; Sun M; Zeng X; Liu J; Liu GY; Luo HY; Zhang X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):61-3. PubMed ID: 14767912
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese family.
    Lv D; Luo Y; Yang W; Cao L; Wen Y; Zhao X; Sun M; Lo WH; Zhang X
    J Hum Genet; 2009 Jul; 54(7):422-5. PubMed ID: 19461659
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A new mutation in the gene ROR2 causes brachydactyly type B1.
    Huang D; Jiang S; Zhang Y; Liu X; Zhang J; He R
    Gene; 2014 Aug; 547(1):106-10. PubMed ID: 24954533
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation screening in candidate genes in four Chinese brachydactyly families.
    Dong S; Wang Y; Tao S; Zheng F
    Ann Clin Lab Sci; 2015; 45(1):94-9. PubMed ID: 25696018
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel variant in the ROR2 gene underlying brachydactyly type B: a case report.
    Shao J; Liu Y; Zhao S; Sun W; Zhan J; Cao L
    BMC Pediatr; 2022 Sep; 22(1):528. PubMed ID: 36064339
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Genetic analysis of a Chinese pedigree affected with Brachydactyly type B1 due to a novel variant of ROR2 gene].
    Ren H; Zhao W; Jiang N; Li S
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 May; 41(5):561-564. PubMed ID: 38684301
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A nonsense mutation in the gene ROR2 underlying autosomal dominant brachydactyly type B.
    Habib R; Amin-Ud-Din M; Ahmad W
    Clin Dysmorphol; 2013 Apr; 22(2):47-50. PubMed ID: 23238279
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Brachydactyly type B1: report of a family with de novo ROR2 mutation.
    Hamamy H; Saleh N; Oldridge M; Al-Hadidy A; Ajlouni K
    Clin Genet; 2006 Dec; 70(6):538-40. PubMed ID: 17101003
    [No Abstract]   [Full Text] [Related]  

  • 10. Distinct mutations in the receptor tyrosine kinase gene ROR2 cause brachydactyly type B.
    Schwabe GC; Tinschert S; Buschow C; Meinecke P; Wolff G; Gillessen-Kaesbach G; Oldridge M; Wilkie AO; Kömec R; Mundlos S
    Am J Hum Genet; 2000 Oct; 67(4):822-31. PubMed ID: 10986040
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A gradient of ROR2 protein stability and membrane localization confers brachydactyly type B or Robinow syndrome phenotypes.
    Schwarzer W; Witte F; Rajab A; Mundlos S; Stricker S
    Hum Mol Genet; 2009 Nov; 18(21):4013-21. PubMed ID: 19640924
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Identification of a pathogenic microduplication in a Chinese split-hand/split-foot malformation family].
    Liu Y; Huang Y; Yang W; Zhang X
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun; 31(3):276-9. PubMed ID: 24928001
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2.
    Afzal AR; Rajab A; Fenske CD; Oldridge M; Elanko N; Ternes-Pereira E; Tüysüz B; Murday VA; Patton MA; Wilkie AO; Jeffery S
    Nat Genet; 2000 Aug; 25(4):419-22. PubMed ID: 10932186
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [A DNA duplication at chromosome 10q24.3 is associated with split-hand split-foot malformation in a Chinese family].
    Yang W; Hu ZJ; Yu XF; Li QH; Zhang AJ; Deng X; Zhang AY; Gao CS; Liu Y; Ao Y; Lo WH; Zhang X
    Zhonghua Yi Xue Za Zhi; 2006 Mar; 86(10):652-8. PubMed ID: 16681918
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel heterozygous mutation in the Indian hedgehog gene (IHH) is associated with brachydactyly type A1 in a Chinese family.
    Liu M; Wang X; Cai Z; Tang Z; Cao K; Liang B; Ren X; Liu JY; Wang QK
    J Hum Genet; 2006; 51(8):727-731. PubMed ID: 16871364
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B.
    Oldridge M; Fortuna AM; Maringa M; Propping P; Mansour S; Pollitt C; DeChiara TM; Kimble RB; Valenzuela DM; Yancopoulos GD; Wilkie AO
    Nat Genet; 2000 Mar; 24(3):275-8. PubMed ID: 10700182
    [TBL] [Abstract][Full Text] [Related]  

  • 17. One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B.
    Afzal AR; Jeffery S
    Hum Mutat; 2003 Jul; 22(1):1-11. PubMed ID: 12815588
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel mutation of p63 in a Chinese family with inherited syndactyly and adactylism.
    Luo T; Yu W; Yuan Z; Deng Y; Zhao Y; Yuan W; Xiao J; Wang Y; Luo N; Mo X; Li Y; Liu M; Wu X
    Mutat Res; 2008 Jan; 637(1-2):182-9. PubMed ID: 17915261
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome.
    van Bokhoven H; Celli J; Kayserili H; van Beusekom E; Balci S; Brussel W; Skovby F; Kerr B; Percin EF; Akarsu N; Brunner HG
    Nat Genet; 2000 Aug; 25(4):423-6. PubMed ID: 10932187
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Exome sequencing reveals a heterozygous DLX5 mutation in a Chinese family with autosomal-dominant split-hand/foot malformation.
    Wang X; Xin Q; Li L; Li J; Zhang C; Qiu R; Qian C; Zhao H; Liu Y; Shan S; Dang J; Bian X; Shao C; Gong Y; Liu Q
    Eur J Hum Genet; 2014 Sep; 22(9):1105-10. PubMed ID: 24496061
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.