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

187 related items for PubMed ID: 11302131

  • 21. Microcephaly-lymphoedema-chorioretinal-dysplasia syndrome with atrial septal defect.
    Strauss RM, Ferguson AD, Rittey CD, Cork MJ.
    Pediatr Dermatol; 2005; 22(4):373-4. PubMed ID: 16060885
    [No Abstract] [Full Text] [Related]

  • 22. A genetic association between microcephaly and lymphedema.
    Meinecke P.
    Am J Med Genet; 1987 Jan; 26(1):233. PubMed ID: 3812570
    [No Abstract] [Full Text] [Related]

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

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

  • 25. A genetic association between microcephaly and lymphedema.
    Crowe CA, Dickerman LH.
    Am J Med Genet; 1986 May; 24(1):131-5. PubMed ID: 3706402
    [Abstract] [Full Text] [Related]

  • 26. Congenital toxoplasmosis mimicking microcephaly-lymphedema-chorioretinal dysplasia.
    Ozeki Y, Shimada Y, Tanikawa A, Horiguchi M, Takeuchi M, Yamazaki T.
    Jpn J Ophthalmol; 2010 Nov; 54(6):626-8. PubMed ID: 21191727
    [No Abstract] [Full Text] [Related]

  • 27. Dominantly inherited syndrome of microcephaly and congenital lymphedema.
    Leung AK.
    Clin Genet; 1985 Jun; 27(6):611-2. PubMed ID: 4017282
    [Abstract] [Full Text] [Related]

  • 28. An autosomal dominant midline cleft syndrome resembling familial holoprosencephaly.
    Martin AO, Perrin JC, Muir WA, Ruch E, Schafer IA.
    Clin Genet; 1977 Aug; 12(2):65-72. PubMed ID: 891015
    [Abstract] [Full Text] [Related]

  • 29. [Genetic heterogeneity in Seckel syndrome].
    Labrune P.
    Arch Pediatr; 2004 Apr; 11(4):368-9. PubMed ID: 15139328
    [No Abstract] [Full Text] [Related]

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

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

  • 32. A syndrome of microcephaly and retinal pigmentary abnormalities without mental retardation in a family with coincidental autosomal dominant hyperreflexia.
    Parke JT, Riccardi VM, Lewis RA, Ferrell RE.
    Am J Med Genet; 1984 Mar; 17(3):585-94. PubMed ID: 6711609
    [Abstract] [Full Text] [Related]

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

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. Cohen syndrome: report of nine cases and review of the literature, with emphasis on ophthalmic features.
    Taban M, Memoracion-Peralta DS, Wang H, Al-Gazali LI, Traboulsi EI.
    J AAPOS; 2007 Oct; 11(5):431-7. PubMed ID: 17383910
    [Abstract] [Full Text] [Related]

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

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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