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115 related items for PubMed ID: 3779537

  • 1. X-linked hydrocephalus.
    Kuzniecky RI, Watters GV, Watters L, Meagher-Villemure K.
    Can J Neurol Sci; 1986 Nov; 13(4):344-6. PubMed ID: 3779537
    [Abstract] [Full Text] [Related]

  • 2. Aqueductal stenosis in X-linked hydrocephalus: a secondary phenomenon?
    Landrieu P, Ninane J, Ferrière G, Lyon G.
    Dev Med Child Neurol; 1979 Oct; 21(5):637-42. PubMed ID: 574474
    [Abstract] [Full Text] [Related]

  • 3. Prenatal diagnosis of X linked hydrocephalus without aqueductal stenosis.
    Váradi V, Csécsei K, Szeifert GT, Tóth Z, Papp Z.
    J Med Genet; 1987 Apr; 24(4):207-9. PubMed ID: 3295245
    [Abstract] [Full Text] [Related]

  • 4. Congenital hydrocephalus and clasped thumbs: two cases of brothers in a family.
    Mochizuki Y, Suyehiro Y, Ihara Y, Tomimoto K, Saito A, Ito T.
    Brain Dev; 1981 Apr; 3(4):407-9. PubMed ID: 7316097
    [Abstract] [Full Text] [Related]

  • 5. Genetic heterogeneity in X-linked hydrocephalus: linkage to markers within Xq27.3.
    Strain L, Gosden CM, Brock DJ, Bonthron DT.
    Am J Hum Genet; 1994 Feb; 54(2):236-43. PubMed ID: 8304340
    [Abstract] [Full Text] [Related]

  • 6. Prenatal diagnosis of hydrocephalus-stenosis of the aqueduct of Sylvius by ultrasound in the first trimester of pregnancy. Report of two cases.
    Senat MV, Bernard JP, Delezoide A, Saugier-Veber P, Hillion Y, Roume J, Ville Y.
    Prenat Diagn; 2001 Dec; 21(13):1129-32. PubMed ID: 11787037
    [Abstract] [Full Text] [Related]

  • 7. X linked hydrocephalus: a survey of a 20 year period in Victoria, Australia.
    Halliday J, Chow CW, Wallace D, Danks DM.
    J Med Genet; 1986 Feb; 23(1):23-31. PubMed ID: 3950933
    [Abstract] [Full Text] [Related]

  • 8. X-linked hydrocephalus: clinical heterogeneity at a single gene locus.
    Serville F, Lyonnet S, Pelet A, Reynaud M, Louail C, Munnich A, Le Merrer M.
    Eur J Pediatr; 1992 Jul; 151(7):515-8. PubMed ID: 1396913
    [Abstract] [Full Text] [Related]

  • 9. Congenital hydrocephalus internus and aqueduct stenosis: aetiology and implications for genetic counselling.
    Haverkamp F, Wölfle J, Aretz M, Krämer A, Höhmann B, Fahnenstich H, Zerres K.
    Eur J Pediatr; 1999 Jun; 158(6):474-8. PubMed ID: 10378395
    [Abstract] [Full Text] [Related]

  • 10. 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 Jun; 5(1):1-10. PubMed ID: 8031529
    [Abstract] [Full Text] [Related]

  • 11. X-linked hydrocephalus.
    Willems PJ, Brouwer OF, Dijkstra I, Wilmink J.
    Am J Med Genet; 1987 Aug; 27(4):921-8. PubMed ID: 3425602
    [Abstract] [Full Text] [Related]

  • 12. X-linked hydrocephalus masquerading as spina bifida and destructive porencephaly in successive generations in one family.
    Brewer CM, Fredericks BJ, Pont JM, Stephenson JB, Tolmie JL.
    Dev Med Child Neurol; 1996 Jul; 38(7):632-6. PubMed ID: 8674913
    [Abstract] [Full Text] [Related]

  • 13. X-linked congenital hydrocephalus.
    Renier WO, Ter Haar BG, Slooff JL, Hustinx TW, Gabreëls FJ.
    Clin Neurol Neurosurg; 1982 Jul; 84(2):113-23. PubMed ID: 6288305
    [Abstract] [Full Text] [Related]

  • 14. [X chromosome recessively transmitted hydrocephalus with congenital aqueduct stenosis].
    Reinthaller A, Deutinger J.
    Z Geburtshilfe Perinatol; 1985 Jul; 189(5):244-6. PubMed ID: 3907171
    [Abstract] [Full Text] [Related]

  • 15. Prenatal exclusion of X-linked hydrocephalus-stenosis of the aqueduct of Sylvius sequence using closely linked DNA markers.
    Serville F, Benit P, Saugier P, Vibert M, Royer G, Pelet A, Chery M, Munnich A, Lyonnet S.
    Prenat Diagn; 1993 Jun; 13(6):435-9. PubMed ID: 8372068
    [Abstract] [Full Text] [Related]

  • 16. X linked complicated spastic paraplegia, MASA syndrome, and X linked hydrocephalus owing to congenital stenosis of the aqueduct of Sylvius: variable expression of the same mutation at Xq28.
    Fryns JP, Spaepen A, Cassiman JJ, van den Berghe H.
    J Med Genet; 1991 Jun; 28(6):429-31. PubMed ID: 1870106
    [No Abstract] [Full Text] [Related]

  • 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; 8(2):367-70. PubMed ID: 1979056
    [Abstract] [Full Text] [Related]

  • 18. Familial Hydrocephalus and Dysgenesis of the Corpus Callosum Associated with Xp22.33 Duplication and Stenosis of the Aqueduct of Sylvius with X-Linked Recessive Inheritance Pattern.
    Alhousseini A, Zeineddine S, Husseini A, Baddah H, Saker H, Mody S, Ibrahim SA, Thakur M, Hernandez-Andrade E, Bahado-Singh R.
    Gynecol Obstet Invest; 2019 Oct; 84(4):412-416. PubMed ID: 30965333
    [Abstract] [Full Text] [Related]

  • 19. Familial congenital hydrocephalus and aqueduct stenosis with probably autosomal dominant inheritance and variable expression.
    Verhagen WI, Bartels RH, Fransen E, van Camp G, Renier WO, Grotenhuis JA.
    J Neurol Sci; 1998 Jun 11; 158(1):101-5. PubMed ID: 9667786
    [Abstract] [Full Text] [Related]

  • 20. X-linked recessive aqueductal stenosis without macrocephaly.
    Kelley RI, Mennuti MT, Hickey WF, Zackai EH.
    Clin Genet; 1988 May 11; 33(5):390-4. PubMed ID: 3378368
    [Abstract] [Full Text] [Related]

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