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Journal Abstract Search

143 related items for PubMed ID: 11450388

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

  • 2. 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
    [Abstract] [Full Text] [Related]

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

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

  • 5. 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 Mar; 53(1):40-4. PubMed ID: 19878742
    [Abstract] [Full Text] [Related]

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

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

  • 8. [Roberts-SC phocomelia syndrome].
    Kawame H.
    Ryoikibetsu Shokogun Shirizu; 2000 Mar; (30 Pt 5):234-5. PubMed ID: 11057210
    [No Abstract] [Full Text] [Related]

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  • 10. 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
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  • 12. A lethal, unclassifiable form of micromelic dwarfism with posterior cleft palate, multiple cervicothoracal vertebral anomalies and iliac hypoplasia: evidence for autosomal recessive inheritance.
    Fryns JP, Moerman P.
    Genet Couns; 1998 Feb; 9(1):61-2. PubMed ID: 9555592
    [No Abstract] [Full Text] [Related]

  • 13. Limb/pelvis hypoplasia/aplasia with skull defect (Schinzel phocomelia): distinctive features and prenatal detection.
    Olney RS, Hoyme HE, Roche F, Ferguson K, Hintz S, Madan A.
    Am J Med Genet; 2001 Nov 01; 103(4):295-301. PubMed ID: 11746009
    [Abstract] [Full Text] [Related]

  • 14. [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 01; 29(3):239-43. PubMed ID: 3057982
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  • 16. Limb reduction defects and renal dysplasia: confirmation of a new, apparently lethal, autosomal recessive MCA syndrome.
    Schrander-Stumpel C, de Die-Smulders C, Fryns JP, da Costa J, Bouckaert P.
    Am J Med Genet; 1990 Sep 01; 37(1):133-5. PubMed ID: 2240030
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  • 18. 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 01; 37(1):18-22. PubMed ID: 2240038
    [Abstract] [Full Text] [Related]

  • 19. [Genetic morphological fatal syndromes. The Fryns syndrome].
    Henkel KE, Pfeiffer RA, Stöss H.
    Pathologe; 1993 Mar 01; 14(2):92-3. PubMed ID: 8469652
    [No Abstract] [Full Text] [Related]

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