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Journal Abstract Search

216 related items for PubMed ID: 8062432

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  • 6. Agenesis of the corpus callosum associated with MASA syndrome.
    Boyd E, Schwartz CE, Schroer RJ, May MM, Shapiro SD, Arena JF, Lubs HA, Stevenson RE.
    Clin Dysmorphol; 1993 Oct; 2(4):332-41. PubMed ID: 8305964
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  • 12. X-linked mental retardation with bilateral clasped thumbs: report of another affected family.
    Straussberg R, Blatt I, Brand N, Kessler D, Katznelson MB, Goodman RM.
    Clin Genet; 1991 Nov; 40(5):337-41. PubMed ID: 1756607
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  • 13. The spectrum of "complicated spastic paraplegia, MASA syndrome and X-linked hydrocephalus". Contribution of DNA linkage analysis in genetic counseling of individual families.
    Schrander-Stumpel C, Meyer H, Merckx D, Jones M, Israel J, Sommer A, Stevens C, Tinschert S, Wilson G, Willems P.
    Genet Couns; 1994 Nov; 5(1):1-10. PubMed ID: 8031529
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  • 14. MASA syndrome: clinical variability and linkage analysis.
    Rietschel M, Friedl W, Uhlhaas S, Neugebauer M, Heimann D, Zerres K.
    Am J Med Genet; 1991 Oct 01; 41(1):10-4. PubMed ID: 1951449
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  • 15. Refining the genetic location of the gene for X linked hydrocephalus within Xq28.
    Jouet M, Feldman E, Yates J, Donnai D, Paterson J, Siggers D, Kenwrick S.
    J Med Genet; 1993 Mar 01; 30(3):214-7. PubMed ID: 8474107
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  • 16. Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28.
    Biancalana V, Le Marec B, Odent S, van den Hurk JA, Hanauer A.
    Hum Genet; 1991 Dec 01; 88(2):228-30. PubMed ID: 1757098
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  • 17. Assignment of X-linked hydrocephalus to Xq28 by linkage analysis.
    Willems PJ, Dijkstra I, Van der Auwera BJ, Vits L, Coucke P, Raeymaekers P, Van Broeckhoven C, Consalez GG, Freeman SB, Warren ST.
    Genomics; 1990 Oct 01; 8(2):367-70. PubMed ID: 1979056
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  • 18. Spectrum of X-linked hydrocephalus (HSAS), MASA syndrome, and complicated spastic paraplegia (SPG1): Clinical review with six additional families.
    Schrander-Stumpel C, Höweler C, Jones M, Sommer A, Stevens C, Tinschert S, Israel J, Fryns JP.
    Am J Med Genet; 1995 May 22; 57(1):107-16. PubMed ID: 7645588
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  • 19. [The MASA syndrome (Mental retardation, Aphasia, Spastic paraplegia and Adducted thumbs), is it heterogeneous?].
    Stoll C, Alembik Y, Pfindel M, Chauvin A, Hanauer A.
    Arch Fr Pediatr; 1993 Oct 22; 50(8):665-9. PubMed ID: 7516145
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  • 20. Linkage to Xq28 in a family with nonspecific X-linked mental retardation.
    Nordström AM, Penttinen M, von Koskull H.
    Hum Genet; 1992 Nov 22; 90(3):263-6. PubMed ID: 1362558
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