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 *

89 related articles for article (PubMed ID: 15909866)

  • 1. Tel-Hashomer camptodactyly syndrome with hirsuitism in an Indian family.
    Patel ZM; Adhia RA
    J Assoc Physicians India; 2004 Oct; 52():837-8. PubMed ID: 15909866
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Two siblings with Tel Hashomer camptodactyly and mitral valve prolapse.
    Toriello HV; Higgins JV; Malvitz T; Waterman DF
    Am J Med Genet; 1990 Aug; 36(4):398-403. PubMed ID: 2202212
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Inguinal hernia and atrial septal defect in Tel Hashomer camptodactyly syndrome: report of a new case expanding the phenotypic spectrum of the disease.
    Franceschini P; Vardeu MP; Signorile F; Testa A; Guala A; Franceschini D; Dalforno L
    Am J Med Genet; 1993 May; 46(3):341-4. PubMed ID: 8488882
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Three new cases of Tel Hashomer camptodactyly syndrome in one Arabic family.
    Tylki-Szymanska A
    Am J Med Genet; 1986 Mar; 23(3):759-63. PubMed ID: 3953674
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The status of dermatoglyphics as a biomarker of Tel Hashomer camptodactyly syndrome: a review of the literature.
    Wijerathne BT; Meier RJ; Agampodi SB
    J Med Case Rep; 2016 Sep; 10(1):258. PubMed ID: 27650795
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [The Tel Hashomer camptodactyly syndrome].
    Rogovina EG; Aver'ianov IuN; Nechkina NP; Logunova LV
    Zh Nevrol Psikhiatr Im S S Korsakova; 1995; 95(4):83-6. PubMed ID: 8533519
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Tel Hashomer camptodactyly syndrome in a consanguineous Brazilian family.
    Gollop TR; Colletto GM
    Am J Med Genet; 1984 Feb; 17(2):399-406. PubMed ID: 6702893
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Tel Hashomer camptodactyly syndrome: a case report.
    Shah K; Sreekanth R; Thomas B; Danda S
    West Indian Med J; 2013 Jan; 62(1):81-3. PubMed ID: 24171333
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel truncating variant in the FGD1 gene associated with Aarskog-Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactyly.
    Kessel I; German A; Peleg A; ; Gonzaga-Jauregui C; Paperna T; Ekhilevitch N; Kurolap A; Baris Feldman H; Sagi-Dain L
    Am J Med Genet A; 2021 Oct; 185(10):3161-3166. PubMed ID: 34145742
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cloning and characterization of the novel chimeric gene TEL/PTPRR in acute myelogenous leukemia with inv(12)(p13q13).
    Nakamura F; Nakamura Y; Maki K; Sato Y; Mitani K
    Cancer Res; 2005 Aug; 65(15):6612-21. PubMed ID: 16061641
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Tel Hashomer camptodactyly syndrome: report of a new case and review of the literature.
    Pagnan NA; Gollop TR; Lederman H
    Am J Med Genet; 1988 Feb; 29(2):411-7. PubMed ID: 3281460
    [TBL] [Abstract][Full Text] [Related]  

  • 12. ETV6 gene rearrangements in invasive breast carcinoma.
    Letessier A; Ginestier C; Charafe-Jauffret E; Cervera N; Adélaïde J; Gelsi-Boyer V; Ahomadegbe JC; Benard J; Jacquemier J; Birnbaum D; Chaffanet M
    Genes Chromosomes Cancer; 2005 Sep; 44(1):103-8. PubMed ID: 15887243
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Extending the spectrum of distal arthrogryposis.
    Gripp KW; Scott CI; Brockett BC; Nicholson L; Mackenzie WG
    Am J Med Genet; 1996 Nov; 65(4):286-90. PubMed ID: 8923937
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mental retardation with blepharo-naso-facial abnormalities and hand malformations: a new syndrome?
    van Maldergem L; Wetzburger C; Verloes A; Fourneau C; Gillerot Y
    Clin Genet; 1992 Jan; 41(1):22-4. PubMed ID: 1633641
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Is Tel Hashomer camptodactyly a distinct clinical entity?
    Mochizuki A; Hyland J; Brown T; Slavin TP
    Am J Med Genet A; 2015 Jan; 167A(1):255-8. PubMed ID: 25348902
    [No Abstract]   [Full Text] [Related]  

  • 16. TEL rearrangements in acute lymphoblastic leukemia: association with p16 deletions in relapsed cases.
    Nomdedéu JF; Badell I; Estivill C; Carnicer MJ; Sierra J; Baiget M
    Haematologica; 2001 May; 86(5):547-8. PubMed ID: 11410424
    [No Abstract]   [Full Text] [Related]  

  • 17. A new observation of two cases of acrofacial dysostosis type Genée-Wiedemann in a family--remarks on the mode of inheritance: report on two sibs.
    Neumann L; Pelz J; Kunze J
    Am J Med Genet; 1996 Sep; 64(4):556-62. PubMed ID: 8870922
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Holt-Oram syndrome. Review and report of 2 clinical cases in a family].
    Lima M
    Rev Port Cardiol; 1995 Mar; 14(3):265-6. PubMed ID: 7646665
    [No Abstract]   [Full Text] [Related]  

  • 19. Identification of the nuclear localization motif in the ETV6 (TEL) protein.
    Park H; Seo Y; Kim JI; Kim WJ; Choe SY
    Cancer Genet Cytogenet; 2006 Jun; 167(2):117-21. PubMed ID: 16737910
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of ectrodactyly and distal phocomelia.
    Delrue MA; Lacombe D
    Genet Couns; 2002; 13(3):319-25. PubMed ID: 12416640
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.