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

254 related items for PubMed ID: 9679615

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

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. Callosal defect, microcephaly, severe mental retardation, and other anomalies in three sibs.
    da-Silva EO.
    Am J Med Genet; 1988 Apr; 29(4):837-43. PubMed ID: 3400727
    [Abstract] [Full Text] [Related]

  • 28. 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]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. [FG syndrome in 2 half brothers].
    Wieg C, Meinecke P.
    Monatsschr Kinderheilkd; 1991 Oct 01; 139(10):687-9. PubMed ID: 1961207
    [Abstract] [Full Text] [Related]

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

  • 34. A new locus for Seckel syndrome on chromosome 18p11.31-q11.2.
    Børglum AD, Balslev T, Haagerup A, Birkebaek N, Binderup H, Kruse TA, Hertz JM.
    Eur J Hum Genet; 2001 Oct 01; 9(10):753-7. PubMed ID: 11781686
    [Abstract] [Full Text] [Related]

  • 35. Apparently new autosomal recessive syndrome of mental retardation, distal limb deficiencies, oral involvement, and possible renal defect.
    Buttiens M, Fryns JP.
    Am J Med Genet; 1987 Jul 01; 27(3):651-60. PubMed ID: 3631136
    [Abstract] [Full Text] [Related]

  • 36. X-linked microcephaly, microphthalmia, microcornea, congenital cataract, hypogenitalism, mental deficiency, growth retardation, spasticity: possible new syndrome.
    Seemanová E, Lesný I.
    Am J Med Genet; 1996 Dec 11; 66(2):179-83. PubMed ID: 8958326
    [Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. [A new variety of dystrophic intra-uterine nanism: Smith, Lemli and Opitz syndrome].
    Zucker JM, Job JC, Rossier A.
    Ann Pediatr (Paris); 1967 Oct 02; 14(10):2409-11. PubMed ID: 5621831
    [No Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 13.