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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

159 related items for PubMed ID: 6544388

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  • 2. A syndrome with true anophthalmia, hand-foot defects and mental retardation.
    Traboulsi EI.
    Ophthalmic Paediatr Genet; 1984 Dec; 4(3):203. PubMed ID: 6545399
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  • 3. 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
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  • 6. Apparent Lenz microphthalmia syndrome: a patient with unusual manifestations.
    Okumus N, Zenciroglu A, Demirel N, Bas AY, Ceylaner S.
    Genet Couns; 2008 Jul 15; 19(2):177-82. PubMed ID: 18618992
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  • 7. Ophthalmo-acromelic syndrome: report and review.
    Tekin M, Tutar E, Arsan S, Atay G, Bodurtha J.
    Am J Med Genet; 2000 Jan 17; 90(2):150-4. PubMed ID: 10607955
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  • 10. [Goltz syndrome. Presentation of 2 cases].
    Pascual-Castroviejo I, Luengo dos Santos A, Baguero Paret G.
    An Esp Pediatr; 1982 Jun 17; 16(6):524-6. PubMed ID: 7125405
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  • 14. Bilateral congenital anophthalmos and agenesis of the optic pathways.
    Aktekin M, Oz O, Saygili MR, Kurtoğlu Z.
    Yonsei Med J; 2005 Apr 30; 46(2):296-9. PubMed ID: 15861506
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  • 17. A second patient with Tsukahara syndrome: type A1 brachydactyly, short stature, hearing loss, microcephaly, mental retardation and ptosis.
    Utine GE, Breckpot J, Thienpont B, Alanay Y, Aksoy C, Boduroğlu K, Devriendt K.
    Am J Med Genet A; 2010 Apr 30; 152A(4):947-9. PubMed ID: 20358606
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  • 19. Short stature, microcephaly, characteristic face, syndactyly and mental retardation: the Filippi syndrome. Report on a second family.
    Meinecke P.
    Genet Couns; 1993 Apr 30; 4(2):147-51. PubMed ID: 8395190
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