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 *

135 related articles for article (PubMed ID: 8832138)

  • 1. A mild form of Roberts/SC phocomelia syndrome with asymmetrical reduction of the upper limbs.
    Concolino D; Sperlì D; Cinti R; Strisciuglio P; Andria G
    Clin Genet; 1996 May; 49(5):274-6. PubMed ID: 8832138
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Roberts syndrome: study of 4 new Rgyptian cases with comparison of clinical and cytogenetic findings.
    Temtamy SA; Ismail S; Helmy NA
    Genet Couns; 2006; 17(1):1-13. PubMed ID: 16719272
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cytogenetic findings in Roberts-SC phocomelia syndrome(s).
    Tomkins D; Hunter A; Roberts M
    Am J Med Genet; 1979; 4(1):17-26. PubMed ID: 495649
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phocomelia, ectrodactyly, skull defect and urinary system anomaly: Schinzel-phocomelia syndrome?
    Evliyaoğlu N; Temoçin AK; Altintaş DU; Duman N; Satar N; Süleymanova D
    Clin Genet; 1996 Feb; 49(2):70-3. PubMed ID: 8740915
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The Roberts syndrome/SC phocomelia spectrum--a case report of an adult with review of the literature.
    Goh ES; Li C; Horsburgh S; Kasai Y; Kolomietz E; Morel CF
    Am J Med Genet A; 2010 Feb; 152A(2):472-8. PubMed ID: 20101700
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The importance of chromosome studies in Roberts syndrome/SC phocomelia and other cohesinopathies.
    Gerkes EH; van der Kevie-Kersemaekers AM; Yakin M; Smeets DF; van Ravenswaaij-Arts CM
    Eur J Med Genet; 2010; 53(1):40-4. PubMed ID: 19878742
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Roberts-SC phocomelia syndrome].
    Musfeld DA; Bühler EM; Heinzl S
    Gynakol Geburtshilfliche Rundsch; 2001; 41(1):3-7. PubMed ID: 11423730
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Roberts syndrome, normal cell division, and normal intelligence.
    Hwang K; Lee DK; Lee SI; Lee HS
    J Craniofac Surg; 2002 May; 13(3):390-4. PubMed ID: 12040206
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Roberts-SC phocomelia syndrome: a case with additional anomalies.
    Satar M; Atici A; Bişak U; Tunali N
    Clin Genet; 1994 Feb; 45(2):107-8. PubMed ID: 8004795
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Prenatal detection of Roberts-SC phocomelia syndrome: report of 2 sibs with characteristic manifestations.
    Robins DB; Ladda RL; Thieme GA; Boal DK; Emanuel BS; Zackai EH
    Am J Med Genet; 1989 Mar; 32(3):390-4. PubMed ID: 2658590
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Roberts-SC phocomelia syndrome.
    Maheshwari A; Kumar P; Dutta S; Narang A
    Indian J Pediatr; 2001 Jun; 68(6):557-9. PubMed ID: 11450388
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [The Roberts-SC phocomelia syndrome. Apropos of a case without cytogenetic changes and review of the literature].
    López-Herce J; Rodríguez Sánchez C; Duelo M; Fontoura M; González M; Gracia R; Oliver A; Peralta A
    An Esp Pediatr; 1985 Dec; 23(8):588-92. PubMed ID: 3006564
    [No Abstract]   [Full Text] [Related]  

  • 13. [Roberts-SC phocomelia syndrome: cytogenetic findings and clinical variability in three brothers].
    Antiñolo Gil G; Borrego López S; Cañadas García de León M; Sánchez García J
    An Esp Pediatr; 1988 Sep; 29(3):239-43. PubMed ID: 3057982
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Prenatal sonographic features and management of a fetus with Roberts-SC phocomelia syndrome (pseudothalidomide syndrome) and pulmonary hypoplasia.
    Sherer DM; Shah YG; Klionsky N; Woods JR
    Am J Perinatol; 1991 Jul; 8(4):259-62. PubMed ID: 1741870
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Roberts-SC phocomelia syndrome with exencephaly.
    Verloes A; Herens C; Van Maldergem L; Retz MC; Dodinval P
    Ann Genet; 1989; 32(3):169-70. PubMed ID: 2817778
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hypopigmented patches in Roberts/SC phocomelia syndrome occur via aneuploidy susceptibility.
    Sezer A; Kayhan G; Zenker M; Percin EF
    Eur J Med Genet; 2019 Dec; 62(12):103608. PubMed ID: 30590172
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Baller-Gerold syndrome: case report and clinical and radiological review.
    Dallapiccola B; Zelante L; Mingarelli R; Pellegrino M; Bertozzi V
    Am J Med Genet; 1992 Feb; 42(3):365-8. PubMed ID: 1536180
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Picture of the month. Roberts-SC phocomelia syndrome.
    Lopez-Allen G; Hutcheon RG; Shaham M; Tunnessen WW
    Arch Pediatr Adolesc Med; 1996 Jun; 150(6):645-6. PubMed ID: 8646318
    [No Abstract]   [Full Text] [Related]  

  • 19. Elaboration of the phenotypic changes of the upper limbs in the Neu-Laxova syndrome.
    Shved IA; Lazjuk GI; Cherstvoy ED
    Am J Med Genet; 1985 Jan; 20(1):1-11. PubMed ID: 3970062
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A sibship with Roberts/SC phocomelia syndrome.
    Holmes-Siedle M; Seres-Santamaria A; Crocker M; Hall JG; Crouchman M
    Am J Med Genet; 1990 Sep; 37(1):18-22. PubMed ID: 2240038
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.