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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

202 related items for PubMed ID: 1785638

  • 21. Two female siblings with a previously unreported MCA/MR syndrome: pre- and postnatal growth retardation, iris colobomata, spasticity, facial dysmorphism and dilated ventricles.
    Yüksel A, Seven M, Deviren A, Söylemez MA, Hacihanefioğlu S, Ulutin T, Cenani A.
    Genet Couns; 1999; 10(3):265-9. PubMed ID: 10546098
    [Abstract] [Full Text] [Related]

  • 22. Delineation of the da-Silva syndrome.
    Naritomi K, Tohma T, Goya Y, Shiroma N, Hirayama K.
    Am J Med Genet; 1994 Feb 01; 49(3):313-6. PubMed ID: 8209892
    [Abstract] [Full Text] [Related]

  • 23. Mental deficiency, alterations in performance, and CNS abnormalities in overgrowth syndromes.
    Cohen MM.
    Am J Med Genet C Semin Med Genet; 2003 Feb 15; 117C(1):49-56. PubMed ID: 12561058
    [Abstract] [Full Text] [Related]

  • 24. [Anesthetic management in a patient with Simpson-Golabi-Behmel syndrome].
    Tsuchiya K, Takahata O, Sengoku K, Hamada I, Suzuki A, Iwasaki H.
    Masui; 2001 Oct 15; 50(10):1106-8. PubMed ID: 11712343
    [Abstract] [Full Text] [Related]

  • 25. Expanding the clinical picture of Simpson-Golabi-Behmel syndrome.
    Young EL, Wishnow R, Nigro MA.
    Pediatr Neurol; 2006 Feb 15; 34(2):139-42. PubMed ID: 16458828
    [Abstract] [Full Text] [Related]

  • 26. Brief cytogenetic case report: a 4.5-year-old girl with deletion 4q syndrome--de novo, 46,XX, del(4) (pter leads to q31:).
    Young RS, Palmer CG, Bender HA, Weaver DD, Hodes ME.
    Am J Med Genet; 1982 May 15; 12(1):103-7. PubMed ID: 7091193
    [No Abstract] [Full Text] [Related]

  • 27. Lambotte syndrome: microcephaly, holoprosencephaly, intrauterine growth retardation, facial anomalies, and early lethality--a new sublethal multiple congenital anomaly/mental retardation syndrome in four sibs.
    Verloes A, Dodinval P, Beco L, Bonnivert J, Lambotte C.
    Am J Med Genet; 1990 Sep 15; 37(1):119-23. PubMed ID: 2240028
    [Abstract] [Full Text] [Related]

  • 28. A third patient with median cleft upper lip, mental retardation and pugilistic facies (W syndrome): corroboration of a hitherto private syndrome.
    Bottani A, Schinzel A.
    Clin Dysmorphol; 1993 Jul 15; 2(3):225-31. PubMed ID: 8287184
    [Abstract] [Full Text] [Related]

  • 29. Morfan: a new syndrome characterized by mental retardation, pre- and postnatal overgrowth, remarkable face and acanthosis nigricans in 5-year-old boy.
    Seemanová E, Rüdiger HW, Dreyer M.
    Am J Med Genet; 1993 Feb 15; 45(4):525-8. PubMed ID: 8465862
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. Leprechaunism (Donohue's syndrome): a case report.
    Tokatli A, Ozsoylu S, Ozme S.
    Turk J Pediatr; 1993 Feb 15; 35(4):319-22. PubMed ID: 8160285
    [Abstract] [Full Text] [Related]

  • 32. A patient with 13q-syndrome with mild mental retardation and with growth retardation.
    Stoll C, Alembik Y.
    Ann Genet; 1998 Feb 15; 41(4):209-12. PubMed ID: 9881184
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. Clinical and molecular overlap in overgrowth syndromes.
    Baujat G, Rio M, Rossignol S, Sanlaville D, Lyonnet S, Le Merrer M, Munnich A, Gicquel C, Colleaux L, Cormier-Daire V.
    Am J Med Genet C Semin Med Genet; 2005 Aug 15; 137C(1):4-11. PubMed ID: 16010674
    [Abstract] [Full Text] [Related]

  • 35. BBBG syndrome or Opitz syndrome: new family.
    Verloes A, Le Merrer M, Briard ML.
    Am J Med Genet; 1989 Nov 15; 34(3):313-6. PubMed ID: 2688419
    [Abstract] [Full Text] [Related]

  • 36. Mental retardation, congenital heart defect, cleft palate, short stature, and facial anomalies: a new X-linked multiple congenital anomalies/mental retardation syndrome: clinical description and molecular studies.
    Hamel BC, Mariman EC, van Beersum SE, Schoonbrood-Lenssen AM, Ropers HH.
    Am J Med Genet; 1994 Jul 15; 51(4):591-7. PubMed ID: 7943045
    [Abstract] [Full Text] [Related]

  • 37. 46,XX/46,XX,del(20)(pter-->p12.2) mosaicism limited to fibroblasts associated with MCA/MR and severe growth deficit.
    Fryns JP, Kleczkowska A, Decock P, Massa G, van den Berghe H.
    Ann Genet; 1992 Jul 15; 35(4):234-6. PubMed ID: 1296522
    [Abstract] [Full Text] [Related]

  • 38. [The Dubowitz syndrome].
    Dumić M, Cvitković M, Letinić D, Filipović-Grcić B, Kordić R.
    Lijec Vjesn; 1994 Jul 15; 116(5-6):135-7. PubMed ID: 7968200
    [Abstract] [Full Text] [Related]

  • 39. Hunter-McAlpine craniosynostosis phenotype associated with skeletal anomalies and interstitial deletion of chromosome 17q.
    Thomas JA, Manchester DK, Prescott KE, Milner R, McGavran L, Cohen MM.
    Am J Med Genet; 1996 Apr 24; 62(4):372-5. PubMed ID: 8723067
    [Abstract] [Full Text] [Related]

  • 40. The dup(3q) syndrome: report of eight cases and review of the literature.
    Steinbach P, Adkins WN, Caspar H, Dumars KW, Gebauer J, Gilbert EF, Grimm T, Habedank M, Hansmann I, Herrmann J, Kaveggia EG, Langenbeck U, Meisner LF, Najafzadeh TM, Opitz JM, Palmer CG, Peters HH, Scholz W, Tavares AS, Wiedeking C.
    Am J Med Genet; 1981 Apr 24; 10(2):159-77. PubMed ID: 7315873
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 11.