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Journal Abstract Search

248 related items for PubMed ID: 8957515

  • 21. Pseudo-trisomy 13 syndrome.
    Cohen MM, Gorlin RJ.
    Am J Med Genet; 1991 Jun 01; 39(3):332-5; discussion 336-7. PubMed ID: 1867286
    [Abstract] [Full Text] [Related]

  • 22. A review of 35 cases of asymmetric crying facies.
    Caksen H, Odabaş D, Tuncer O, Kirimi E, Tombul T, Ikbal M, Ataş B, Ari Yuca S.
    Genet Couns; 2004 Jun 01; 15(2):159-65. PubMed ID: 15287415
    [Abstract] [Full Text] [Related]

  • 23. Campomelia, polycystic dysplasia, and cervical lymphocele in two sibs.
    Urioste M, Arroyo A, Martínez-Frías ML.
    Am J Med Genet; 1991 Dec 15; 41(4):475-7. PubMed ID: 1776641
    [Abstract] [Full Text] [Related]

  • 24. Autosomal recessive Robinow-like syndrome with anterior chamber cleavage anomalies.
    Saal HM, Greenstein RM, Weinbaum PJ, Poole AE.
    Am J Med Genet; 1988 Jul 15; 30(3):709-18. PubMed ID: 3189394
    [Abstract] [Full Text] [Related]

  • 25. The CHARGE association in a newborn infant.
    Akisü M, Ozkinay F, Ozyürek R, Küçüktaş A, Kültürsay N.
    Turk J Pediatr; 1998 Jul 15; 40(2):283-7. PubMed ID: 9714686
    [Abstract] [Full Text] [Related]

  • 26. A child with sclerocornea, short limbs, short stature, and distinct facial appearance.
    Thompson EM, Winter RM.
    Am J Med Genet; 1988 Jul 15; 30(3):719-24. PubMed ID: 3055984
    [Abstract] [Full Text] [Related]

  • 27. Unusual association of congenital malformations: craniosynostosis, heart defect, abnormal intestinal innervation and urogenital abnormalities.
    Van Nesselrooij BP, Spliet W, Beemer FA.
    Clin Dysmorphol; 1998 Jan 15; 7(1):51-3. PubMed ID: 9546831
    [Abstract] [Full Text] [Related]

  • 28. Autosomal recessive syndrome of sacral and conotruncal developmental field defects (Kousseff syndrome).
    Toriello HV, Sharda JK, Beaumont EJ.
    Am J Med Genet; 1985 Oct 15; 22(2):357-60. PubMed ID: 4050868
    [Abstract] [Full Text] [Related]

  • 29. Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation.
    Morava E, Lefeber DJ, Urban Z, de Meirleir L, Meinecke P, Gillessen Kaesbach G, Sykut-Cegielska J, Adamowicz M, Salafsky I, Ranells J, Lemyre E, van Reeuwijk J, Brunner HG, Wevers RA.
    Eur J Hum Genet; 2008 Jan 15; 16(1):28-35. PubMed ID: 17971833
    [Abstract] [Full Text] [Related]

  • 30. Filippi syndrome: report of three additional cases.
    Williams MS, Williams JL, Wargowski DS, Pauli RM, Pletcher BA.
    Am J Med Genet; 1999 Nov 19; 87(2):128-33. PubMed ID: 10533026
    [Abstract] [Full Text] [Related]

  • 31. Roberts syndrome: study of 4 new Rgyptian cases with comparison of clinical and cytogenetic findings.
    Temtamy SA, Ismail S, Helmy NA.
    Genet Couns; 2006 Nov 19; 17(1):1-13. PubMed ID: 16719272
    [Abstract] [Full Text] [Related]

  • 32. Severe case of Al Awadi/Raas-Rothschild syndrome or new, possibly autosomal recessive facio-skeleto-genital syndrome.
    Mollica F, Mazzone D, Cimino G, Opitz JM.
    Am J Med Genet; 1995 Mar 27; 56(2):168-72. PubMed ID: 7625440
    [Abstract] [Full Text] [Related]

  • 33. [The FG syndrome (McK 30545). Description of 2 cases with subaortic stenosis].
    Russo A, Lanna P, Perna GP, Salvatori MP, Villella A, Fanelli R.
    G Ital Cardiol; 1985 Mar 27; 15(3):349-53. PubMed ID: 4040487
    [Abstract] [Full Text] [Related]

  • 34. [Cayler's cardio-facial syndrome. Apropos of 19 cases].
    Perrin P, Worms AM, Marçon F, Perrin C, Pernot C.
    Arch Fr Pediatr; 1989 Apr 27; 46(4):257-61. PubMed ID: 2665683
    [Abstract] [Full Text] [Related]

  • 35. A case of a four-day-old male with Carpenter's syndrome with transposition of great arteries.
    Balci S, Haytoğlu T, Ozer S.
    Turk J Pediatr; 1998 Apr 27; 40(3):461-6. PubMed ID: 9763914
    [Abstract] [Full Text] [Related]

  • 36. Craniosynostosis and kidney malformation in a case of Hennekam syndrome.
    Cormier-Daire V, Lyonnet S, Lehnert A, Martin D, Salomon R, Patey N, Broyer M, Ricour C, Munnich A.
    Am J Med Genet; 1995 May 22; 57(1):66-8. PubMed ID: 7645602
    [Abstract] [Full Text] [Related]

  • 37. Congenital cataract, microphthalmia and septal heart defect in two generations: a new syndrome?
    Wilkie AO, Taylor D, Scambler PJ, Baraitser M.
    Clin Dysmorphol; 1993 Apr 22; 2(2):114-9. PubMed ID: 8281271
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