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: 16131709)

  • 1. Brachydactyly A1: new relatives for old families?
    Girirajan S; Elsea SH
    J Genet; 2005 Aug; 84(2):95-8. PubMed ID: 16131709
    [No Abstract]   [Full Text] [Related]  

  • 2. A second Brachydactylous Family. 1915.
    Drinkwater H
    J Genet; 2005 Aug; 84(2):99-121. PubMed ID: 16131710
    [No Abstract]   [Full Text] [Related]  

  • 3. A century later Farabee has his mutation.
    McCready ME; Grimsey A; Styer T; Nikkel SM; Bulman DE
    Hum Genet; 2005 Jul; 117(2-3):285-7. PubMed ID: 15886999
    [No Abstract]   [Full Text] [Related]  

  • 4. Heterogeneity of the autosomal dominant split hand/split foot malformation.
    Zlotogora J
    Am J Hum Genet; 1995 Jan; 56(1):341-3. PubMed ID: 7825599
    [No Abstract]   [Full Text] [Related]  

  • 5. A novel locus for brachydactyly type A1 on chromosome 5p13.3-p13.2.
    Armour CM; McCready ME; Baig A; Hunter AG; Bulman DE
    J Med Genet; 2002 Mar; 39(3):186-8. PubMed ID: 11897820
    [No Abstract]   [Full Text] [Related]  

  • 6. A case report of brachydactyly types D and E: a new variation of brachydactyly.
    Ridgeway S; Tai CC; Singh D
    Foot Ankle Int; 2004 Jun; 25(6):419-22. PubMed ID: 15215028
    [No Abstract]   [Full Text] [Related]  

  • 7. Answering a century old riddle: brachydactyly type A1.
    Gao B; He L
    Cell Res; 2004 Jun; 14(3):179-87. PubMed ID: 15225411
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A boy with severe manifestations of type A1 brachydactyly.
    Slavotinek A; Donnai D
    Clin Dysmorphol; 1998 Jan; 7(1):21-7. PubMed ID: 9546826
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Split hand foot malformation (SHFM).
    Elliott AM; Evans JA; Chudley AE
    Clin Genet; 2005 Dec; 68(6):501-5. PubMed ID: 16283879
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 50 Years Ago in The Journal of Pediatrics: Hand-Foot-Genital Syndrome and Its Multiple Genetic Mechanisms.
    Giampietro PF
    J Pediatr; 2020 Jul; 222():185. PubMed ID: 32586521
    [No Abstract]   [Full Text] [Related]  

  • 11. Mutations in IHH, encoding Indian hedgehog, cause brachydactyly type A-1.
    Gao B; Guo J; She C; Shu A; Yang M; Tan Z; Yang X; Guo S; Feng G; He L
    Nat Genet; 2001 Aug; 28(4):386-8. PubMed ID: 11455389
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Autosomal dominant hypertension with brachydactyly: an enigmatic form of monogenic hypertension.
    Schuster H
    Nephrol Dial Transplant; 1998 Jun; 13(6):1337-40. PubMed ID: 9641152
    [No Abstract]   [Full Text] [Related]  

  • 13. P63 mutations are not a major cause of non-syndromic split hand/foot malformation.
    de Mollerat XJ; Everman DB; Morgan CT; Clarkson KB; Rogers RC; Colby RS; Aylsworth AS; Graham JM; Stevenson RE; Schwartz CE
    J Med Genet; 2003 Jan; 40(1):55-61. PubMed ID: 12525544
    [No Abstract]   [Full Text] [Related]  

  • 14. The expanding panorama of split hand foot malformation.
    Basel D; Kilpatrick MW; Tsipouras P
    Am J Med Genet A; 2006 Jul; 140(13):1359-65. PubMed ID: 16763964
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Skeletal malformations and polycystic kidney disease.
    Winter RM
    J Med Genet; 1993 Nov; 30(11):973. PubMed ID: 8301661
    [No Abstract]   [Full Text] [Related]  

  • 16. [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]  

  • 17. [Split hand/foot abnormalities: classification, pathogenesis, epidemiology].
    Elek C; Vitéz M; Czeizel E
    Orv Hetil; 1991 Jul; 132(30):1639-42. PubMed ID: 1866158
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Brachydactyly type A1 with abnormal menisci and scoliosis in three generations.
    Raff ML; Leppig KA; Rutledge JC; Weinberger E; Pagon RA
    Clin Dysmorphol; 1998 Jan; 7(1):29-34. PubMed ID: 9546827
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An apparently new mental retardation syndrome in three elderly sisters.
    Viljoen DL; Kallis J; Voges S; Marais AS; van Vuuren I
    Clin Genet; 1991 Jul; 40(1):6-11. PubMed ID: 1884519
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The p63 gene in EEC and other syndromes.
    Brunner HG; Hamel BC; Van Bokhoven H
    J Med Genet; 2002 Jun; 39(6):377-81. PubMed ID: 12070241
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.