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

Journal Abstract Search


142 related items for PubMed ID: 8372068

  • 1. 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]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 4. 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]

  • 5. 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]

  • 6. Autosomal recessive hydrocephalus due to congenital stenosis of the aqueduct of sylvius.
    Hamada H, Watanabe H, Sugimoto M, Yasuoka M, Yamada N, Kubo T.
    Prenat Diagn; 1999 Nov; 19(11):1067-9. PubMed ID: 10589063
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 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. 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; 30(3):214-7. PubMed ID: 8474107
    [Abstract] [Full Text] [Related]

  • 12. The value of early and comprehensive diagnoses in a human fetus with hydrocephalus and progressive obliteration of the aqueduct of Sylvius: Case Report.
    Ortega E, Muñoz RI, Luza N, Guerra F, Guerra M, Vio K, Henzi R, Jaque J, Rodriguez S, McAllister JP, Rodriguez E.
    BMC Neurol; 2016 Apr 11; 16():45. PubMed ID: 27067115
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. [X-linked hydrocephalus. Prenatal diagnosis].
    Conti M, Grossi E, Simoni G, Terzoli GL, Sanchioni L, Pomè G.
    Pathologica; 1983 Jun 11; 75(1035):35-44. PubMed ID: 6683835
    [No Abstract] [Full Text] [Related]

  • 15. [X chromosome recessively transmitted hydrocephalus with congenital aqueduct stenosis].
    Reinthaller A, Deutinger J.
    Z Geburtshilfe Perinatol; 1985 Jun 11; 189(5):244-6. PubMed ID: 3907171
    [Abstract] [Full Text] [Related]

  • 16. Aqueductal stenosis in X-linked hydrocephalus: a secondary phenomenon?
    Landrieu P, Ninane J, Ferrière G, Lyon G.
    Dev Med Child Neurol; 1979 Oct 11; 21(5):637-42. PubMed ID: 574474
    [Abstract] [Full Text] [Related]

  • 17. Neuropathological review of 138 cases genetically tested for X-linked hydrocephalus: evidence for closely related clinical entities of unknown molecular bases.
    Adle-Biassette H, Saugier-Veber P, Fallet-Bianco C, Delezoide AL, Razavi F, Drouot N, Bazin A, Beaufrère AM, Bessières B, Blesson S, Bucourt M, Carles D, Devisme L, Dijoud F, Fabre B, Fernandez C, Gaillard D, Gonzales M, Jossic F, Joubert M, Laurent N, Leroy B, Loeuillet L, Loget P, Marcorelles P, Martinovic J, Perez MJ, Satge D, Sinico M, Tosi M, Benichou J, Gressens P, Frebourg T, Laquerrière A.
    Acta Neuropathol; 2013 Sep 11; 126(3):427-42. PubMed ID: 23820807
    [Abstract] [Full Text] [Related]

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

  • 19. Prenatal molecular diagnosis of a severe type of L1 syndrome (X-linked hydrocephalus).
    Yamasaki M, Nonaka M, Suzumori N, Nakamura H, Fujita H, Namba A, Kamei Y, Yamada T, Pooh RK, Tanemura M, Sudo N, Nagasaka M, Yoshioka E, Shofuda T, Kanemura Y.
    J Neurosurg Pediatr; 2011 Oct 11; 8(4):411-6. PubMed ID: 21961551
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 8.