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

182 related items for PubMed ID: 5173148

  • 1. A family with microphthalmia, anophthalmia and concomitant oligophrenia.
    Bianchine JW.
    Birth Defects Orig Artic Ser; 1971 Mar; 7(3):205-6. PubMed ID: 5173148
    [No Abstract] [Full Text] [Related]

  • 2. Genetic heterogeneity of syndromic X-linked recessive microphthalmia-anophthalmia: is Lenz microphthalmia a single disorder?
    Ng D, Hadley DW, Tifft CJ, Biesecker LG.
    Am J Med Genet; 2002 Jul 15; 110(4):308-14. PubMed ID: 12116202
    [Abstract] [Full Text] [Related]

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

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

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. [SOX2 defect and anophthalmia and microphthalmia].
    Ye FX, Fan XQ.
    Zhonghua Yan Ke Za Zhi; 2012 Nov 15; 48(11):1049-52. PubMed ID: 23302280
    [Abstract] [Full Text] [Related]

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

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

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 11. [Anophthalmia-microphthalmia with dementia and epilepsy as well as osteopathia antieleptica].
    Fehlow P.
    Padiatr Grenzgeb; 1988 Nov 15; 27(4):317-21. PubMed ID: 3174145
    [No Abstract] [Full Text] [Related]

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

  • 13. Unilateral isolated microphthalmia inherited as an autosomal recessive trait.
    Fleckenstein M, Maumenee IH.
    Ophthalmic Genet; 2005 Dec 15; 26(4):163-8. PubMed ID: 16352476
    [Abstract] [Full Text] [Related]

  • 14. Microphthalmia, anophthalmia, and coloboma and associated ocular and systemic features: understanding the spectrum.
    Skalicky SE, White AJ, Grigg JR, Martin F, Smith J, Jones M, Donaldson C, Smith JE, Flaherty M, Jamieson RV.
    JAMA Ophthalmol; 2013 Dec 15; 131(12):1517-24. PubMed ID: 24177921
    [Abstract] [Full Text] [Related]

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

  • 16. Mental retardation and unilateral anophthalmia in hemifacial microsomia.
    Starzak RJ, Fujimoto A.
    Am J Ment Defic; 1980 Nov 15; 85(3):315-7. PubMed ID: 7446601
    [Abstract] [Full Text] [Related]

  • 17. A practical guide to the management of anophthalmia and microphthalmia.
    Ragge NK, Subak-Sharpe ID, Collin JR.
    Eye (Lond); 2007 Oct 15; 21(10):1290-300. PubMed ID: 17914432
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Mutations in ALDH1A3 cause microphthalmia.
    Aldahmesh MA, Khan AO, Hijazi H, Alkuraya FS.
    Clin Genet; 2013 Aug 15; 84(2):128-31. PubMed ID: 23646827
    [Abstract] [Full Text] [Related]

  • 20. Mutations in ALDH1A3 represent a frequent cause of microphthalmia/anophthalmia in consanguineous families.
    Abouzeid H, Favez T, Schmid A, Agosti C, Youssef M, Marzouk I, El Shakankiry N, Bayoumi N, Munier FL, Schorderet DF.
    Hum Mutat; 2014 Aug 15; 35(8):949-53. PubMed ID: 24777706
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.