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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

95 related items for PubMed ID: 5739102

  • 41. [Cerebral gigantism in childhood].
    Schlack HG, Pfeiffer RA.
    Munch Med Wochenschr; 1970 Jan 02; 112(1):26-31. PubMed ID: 5538070
    [No Abstract] [Full Text] [Related]

  • 42. Characteristic facial dysmorphism, arachnodactyly and mental handicap in two unrelated girls: a distinct MCA/MR syndrome?
    de Die-Smulders C, Vles H, Fryns JP.
    Genet Couns; 1993 Jan 02; 4(2):165-7. PubMed ID: 8357568
    [Abstract] [Full Text] [Related]

  • 43. 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 Jan 02; 10(3):265-9. PubMed ID: 10546098
    [Abstract] [Full Text] [Related]

  • 44. Cerebral gigantism.
    Poznanski AK, Manson G, Mellinger RC, Stephenson JN.
    Am Fam Physician GP; 1970 Feb 02; 1(2):76. PubMed ID: 5262929
    [No Abstract] [Full Text] [Related]

  • 45. Abnormal face, congenital absence of the left pericardium, mental retardation, and growth hormone deficiency.
    Boscherini B, Galasso C, Bitti ML.
    Am J Med Genet; 1994 Jan 01; 49(1):111-3. PubMed ID: 8172237
    [No Abstract] [Full Text] [Related]

  • 46. Mental retardation, unusual face, and intrauterine growth retardation: a new recessive syndrome?
    Pitt DB, Rogers JG, Danks DM.
    Am J Med Genet; 1984 Oct 01; 19(2):307-13. PubMed ID: 6542309
    [Abstract] [Full Text] [Related]

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  • 49. [Soto's syndrome (cerebral gigantism)].
    Jović NS, Vranjesević DN, Jović JZ, Marinković DD.
    Srp Arh Celok Lek; 1996 Oct 01; 124(1-2):37-40. PubMed ID: 9102812
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  • 52. [Case of fibrous dysplasia of the bones of the face and the skull associated with mental retardation with epilepsy and unilateral deafness].
    Wintgens M, Roland T, Evrard M.
    Acta Paediatr Belg; 1968 Oct 01; 22(1):29-40. PubMed ID: 5759451
    [No Abstract] [Full Text] [Related]

  • 53. The value of establishing the genetic component in etiology of craniofacial anomalies.
    Stewart RE.
    Birth Defects Orig Artic Ser; 1980 Oct 01; 16(5):27-33. PubMed ID: 7448376
    [No Abstract] [Full Text] [Related]

  • 54. A Turkish case of subcortical/subependymal heterotopia associated with corpus callosum dysgenesis, craniofacial dysmorphism, severe eye abnormalities, and growth-mental retardation.
    Caksen H, Tuncer O, Ataş B, Demirok A, Unal O, Ikbal M, Odabaş D.
    Genet Couns; 2003 Oct 01; 14(3):343-8. PubMed ID: 14577680
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  • 56. Fallot complex, severe mental, and growth retardation: a new autosomal recessive syndrome?
    Bindewald B, Ulmer H, Müller U.
    Am J Med Genet; 1994 Apr 01; 50(2):173-6. PubMed ID: 8010348
    [Abstract] [Full Text] [Related]

  • 57. Male to male transmission of cerebral gigantism.
    Halal F.
    Am J Med Genet; 1982 Aug 01; 12(4):411-9. PubMed ID: 7124794
    [No Abstract] [Full Text] [Related]

  • 58. Crainiofacial anomalies - the dentist's role.
    Steiner M, Clark TJ.
    J Ky Dent Assoc; 1981 Mar 01; 33(2):14-8. PubMed ID: 6939766
    [No Abstract] [Full Text] [Related]

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  • 60. [On 2 cases of partial gigantism associated with vascular malformations].
    Brancadoro P.
    Rev Bras Biol; 1966 Dec 01; 26(4):1261-78. PubMed ID: 5999431
    [No Abstract] [Full Text] [Related]

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