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

95 related items for PubMed ID: 2950815

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

  • 2. The Bannayan syndrome: an autosomal dominant disorder consisting of macrocephaly, lipomas, hemangiomas, and risk for intracranial tumors.
    Higginbottom MC, Schultz P.
    Pediatrics; 1982 May; 69(5):632-4. PubMed ID: 7079022
    [Abstract] [Full Text] [Related]

  • 3. Macrocephaly with hamartomas: Bannayan-Zonana syndrome.
    Miles JH, Zonana J, Mcfarlane J, Aleck KA, Bawle E.
    Am J Med Genet; 1984 Oct; 19(2):225-34. PubMed ID: 6507473
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. A Japanese male infant with the Weaver syndrome.
    Kondo I, Mori Y, Kuwajima K.
    Jinrui Idengaku Zasshi; 1990 Sep; 35(3):257-62. PubMed ID: 2266602
    [Abstract] [Full Text] [Related]

  • 6. [Leopard syndrome with hypertrophic obstructive cardiomyopathy and cerebral arteriovenous malformation. Report of a case].
    Cabañas A, Baduí E, Estañol B, Aguilar F, González N, López J.
    Arch Inst Cardiol Mex; 1985 Sep; 55(2):147-51. PubMed ID: 3161472
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Teebi hypertelorism syndrome: report of a third family.
    Toriello HV, Delp K.
    Clin Dysmorphol; 1994 Oct; 3(4):335-9. PubMed ID: 7894738
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Aminopterin Syndrome Sine Aminopterin (ASSA) syndrome in two siblings: further delineation of the syndrome and review of the literature.
    Krajewska-Walasek M.
    Genet Couns; 1994 Oct; 5(4):345-55. PubMed ID: 7888136
    [Abstract] [Full Text] [Related]

  • 14. Otocephaly-midline malformation association.
    Hersh JH, McChane RH, Rosenberg EM, Powers WH, Corrigan C, Pancratz L.
    Am J Med Genet; 1989 Oct; 34(2):246-9. PubMed ID: 2817004
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. [Intracranial arteriovenous malformation associated with multiple cutaneous follicular hamartoma. A new syndrome].
    Márk I.
    Orv Hetil; 1993 Dec 12; 134(50):2761-7. PubMed ID: 8265125
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Heredofamilial syndrome of mesodermal hamartomas, macrocephaly, and pseudopapilledema.
    Dvir M, Beer S, Aladjem M.
    Pediatrics; 1988 Feb 12; 81(2):287-90. PubMed ID: 3340479
    [Abstract] [Full Text] [Related]

  • 19. Multiple lentigines syndrome in a Nigerian family.
    Kubeyinje EP, Onunu AN, Obasohan AO.
    Trop Geogr Med; 1993 Feb 12; 45(3):135-7. PubMed ID: 8362457
    [Abstract] [Full Text] [Related]

  • 20. Autosomal dominant inheritance of the DeMyer Sequence.
    Jaramillo C, Brandt SK, Jorgenson RJ.
    J Craniofac Genet Dev Biol; 1988 Feb 12; 8(3):199-204. PubMed ID: 3209682
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.