Heterogeneity in familial hydrocephalus
1988; Wiley; Volume: 31; Issue: 2 Linguagem: Inglês
10.1002/ajmg.1320310229
ISSN1096-8628
AutoresPatrick J. Willems, John M. Opitz,
Tópico(s)Fetal and Pediatric Neurological Disorders
ResumoAmerican Journal of Medical GeneticsVolume 31, Issue 2 p. 471-472 Letter to the Editor Heterogeneity in familial hydrocephalus Dr. P. J. Willems, Corresponding Author Dr. P. J. Willems Department of Medical Genetics, University of Antwerp, BelgiumDepartment of Medical Genetics, Universitaire Instelling Antwerpen, Universiteitsplein 1, 2610 Wilrijk, BelgiumSearch for more papers by this authorJohn M. Opitz, John M. Opitz EditorSearch for more papers by this author Dr. P. J. Willems, Corresponding Author Dr. P. J. Willems Department of Medical Genetics, University of Antwerp, BelgiumDepartment of Medical Genetics, Universitaire Instelling Antwerpen, Universiteitsplein 1, 2610 Wilrijk, BelgiumSearch for more papers by this authorJohn M. Opitz, John M. Opitz EditorSearch for more papers by this author First published: October 1988 https://doi.org/10.1002/ajmg.1320310229Citations: 8AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. References Edwards JH, Norman RM, Roberts JM (1961): Sex-linked hydrocephalus: Report of a family with 15 affected members. Arch Dis Child 36: 481–485. Fandre M, Leroux B, Coucrur N, Pennaforte F, Pluot B (1972): Hydrocéphalie liée au sexe. A propos de trios familles distinctes. Arch Fr Pédiatr 29: 778. Hanau J, Franc B, Faivre J, Foncin J-F (1978): Hydrocéphalie génétique liée au sexe. Etude anatomique. Rev Neurol (Paris) 6-7: 437–442. Landrieu P, Ninane J, Ferriere G, Lyon G (1979): Aqueductal stenosis in X-linked hydrocephalus: A secondary phenomenon? Dev Med Child Neurol 21: 637–652. McKusick A (1986): “ Mendelian Inheritance in Men”. The John Hopkins University Press. Needleman HL, Root AW (1963): Sex-linked hydrocephalus. Report of two families, with chromosomal study of two cases. Pediatrics 31: 396–399. Renier WO, ter Haar BGA, Slooff JL, Hustinx TWJ, Gabreëls FJM (1982): X-linked congenital hydrocephalus. Clin Neurol Neurosurg 84: 113–123. Renier WO, Gabreëls FJM, Hustinx TWJ, Thijssen HOM, ter Haar BGA, Kroll WE, Becker H (1983): Cerebellar hypoplasia, communicating hydrocephalus and mental retardation in two brothers and maternal uncle. Brain Dev 5: 41–45. Teebi AS, Naguib KK (1988): Letter to the Editor: Autosomal recessive nonsyndromal hydrocephalus. Am J Med Genet, this issue. Van Egmond-Linden A, Wladimiroff JW, Jahoda MG, Niermeijer MF, Sachs ES, Stefanko S (1983): Prenatal diagnosis of X-linked hydrocephaly. Prenat Diagn 3: 245–248. Váradi V, Csécsei K, Szeifert GT, Tóath Z, Papp Z (1987): Prenatal diagnosis of X-linked hydrocephalus without aqueductal stenosis. J Med Gent 24: 207–209. Willems PJ, Brouwer OF, Dijkstra I, Wilmink J (1987): X-linked hydrocephalus. Am J Med Genet 27: 921–928. Yeatman GW (1984): Mental retardation-clasped thumb syndrome. Am J Med Gent. 17: 339–344. Citing Literature Volume31, Issue2October 1988Pages 471-472 ReferencesRelatedInformation
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