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

127 related items for PubMed ID: 8484398

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. Lujan-Fryns syndrome (X-linked mental retardation with marfanoid habitus): report of three cases and review.
    Lacombe D, Bonneau D, Verloes A, Couet D, Koulischer L, Battin J.
    Genet Couns; 1993; 4(3):193-8. PubMed ID: 8267926
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Ectomorphic habitus, severe mental retardation and characteristic face: a new MCA/MR syndrome?
    Fryns JP, Smeets E, Thiry P, Geutjens J, Vinken L, Van den Berghe H.
    Am J Med Genet; 1994 Jan 01; 49(1):91-3. PubMed ID: 8172258
    [Abstract] [Full Text] [Related]

  • 5. An unusual syndrome with mental retardation and sparse hair.
    Nicolaides P, Baraitser M.
    Clin Dysmorphol; 1993 Jul 01; 2(3):232-6. PubMed ID: 8287185
    [Abstract] [Full Text] [Related]

  • 6. De novo 18q deletion with mitral valve insufficiency.
    Gunes S, Okten G, Kara N, Saglam Y, Tasdemir HA, Kayacik OE, Tural S.
    Genet Couns; 2008 Jul 01; 19(3):261-5. PubMed ID: 18990980
    [Abstract] [Full Text] [Related]

  • 7. Mental retardation, mitral valve prolapse, and characteristic face: another report?
    Fryer A.
    Am J Med Genet; 1994 Jul 01; 51(3):277-8. PubMed ID: 8074158
    [No Abstract] [Full Text] [Related]

  • 8. Brachytelephalangy with mental retardation, peculiar face and short stature in two sibs. A new MCA/MR syndrome?
    Mégarbané A, Abi Moussa M.
    Genet Couns; 1997 Jul 01; 8(2):127-32. PubMed ID: 9219011
    [Abstract] [Full Text] [Related]

  • 9. [New hereditary syndrome with mental retardation].
    Marincheva GS, Kupriianova TA, Batienko GS.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1988 Jul 01; 88(3):69-74. PubMed ID: 3381618
    [Abstract] [Full Text] [Related]

  • 10. Brief clinical report: two children with de novo del(9p).
    Young RS, Bader P, Palmer CG, Kaler SG, Hodes ME.
    Am J Med Genet; 1983 Apr 01; 14(4):751-7. PubMed ID: 6846405
    [Abstract] [Full Text] [Related]

  • 11. The KBG syndrome: an additional sporadic case.
    Mathieu M, Helou M, Morin G, Dolhem P, Devauchelle B, Piussan C.
    Genet Couns; 2000 Apr 01; 11(1):33-5. PubMed ID: 10756425
    [Abstract] [Full Text] [Related]

  • 12. [Beuren-Williams syndrome and mitral prolapse].
    Luna G, Hernaiz S, Redondo JM, Arribas A, Castaño L.
    Rev Clin Esp; 1985 Feb 01; 176(3):149-51. PubMed ID: 3991961
    [No Abstract] [Full Text] [Related]

  • 13. Mitral valve prolapse and aortic dilatation in the fragile X syndrome.
    Hagerman RJ, Synhorst DP.
    Am J Med Genet; 1984 Jan 01; 17(1):123-31. PubMed ID: 6711591
    [Abstract] [Full Text] [Related]

  • 14. Novel findings in a patient with Weaver or a Weaver-like syndrome.
    Scarano G, Della Monica M, Lonardo F, Neri G.
    Am J Med Genet; 1996 May 17; 63(2):378-81. PubMed ID: 8725789
    [Abstract] [Full Text] [Related]

  • 15. [Mitral prolapse and the Holt-Oram syndrome. Study of a family].
    Masotti G, Ieri A, Castellani S.
    Cardiol Prat; 1978 May 17; 29(2):105-10. PubMed ID: 753519
    [No Abstract] [Full Text] [Related]

  • 16. Kabuki make-up (Niikawa-Kuroki) syndrome in five Spanish children.
    Galán-Gómez E, Cardesa-García JJ, Campo-Sampedro FM, Salamanca-Maesso C, Martínez-Frías ML, Frías JL.
    Am J Med Genet; 1995 Nov 20; 59(3):276-82. PubMed ID: 8599349
    [Abstract] [Full Text] [Related]

  • 17. Spondyloperipheral dysplasia.
    Sorge G, Ruggieri M, Lachman RS.
    Am J Med Genet; 1995 Nov 06; 59(2):139-42. PubMed ID: 8588574
    [Abstract] [Full Text] [Related]

  • 18. Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay.
    Feingold M, Hall BD, Lacassie Y, Martínez-Frías ML.
    Am J Med Genet; 1997 Mar 31; 69(3):245-9. PubMed ID: 9096752
    [Abstract] [Full Text] [Related]

  • 19. Aortic root dilatation and mitral valve prolapse in the fragile X syndrome.
    Loehr JP, Synhorst DP, Wolfe RR, Hagerman RJ.
    Am J Med Genet; 1986 Mar 31; 23(1-2):189-94. PubMed ID: 3953647
    [Abstract] [Full Text] [Related]

  • 20. Williams syndrome in adults.
    Lopez-Rangel E, Maurice M, McGillivray B, Friedman JM.
    Am J Med Genet; 1992 Dec 01; 44(6):720-9. PubMed ID: 1481839
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.