Title: Lack of mutations in ZIC3 in three families with neural tube defects
Abstract: American Journal of Medical GeneticsVolume 98, Issue 3 p. 283-285 Letter to the Editor: Letter to the Editor Lack of mutations in ZIC3 in three families with neural tube defects Tessa Carrel, Tessa Carrel Children’s Research Institute and Department of Pediatrics, Ohio State University, Columbus, OhioSearch for more papers by this authorGail E. Herman, Corresponding Author Gail E. Herman [email protected] Children’s Research Institute and Department of Pediatrics, Ohio State University, Columbus, OhioChildren's Research Institute, 700 Children's Dr. Rm. W403, Columbus, OH 43205.Search for more papers by this authorGudrun E. Moore, Gudrun E. Moore Division of Paediatrics, Obsterics, and Gynaecology, Imperical College School of Medicine, London, UKSearch for more papers by this authorPhilip Stanier, Philip Stanier Division of Paediatrics, Obsterics, and Gynaecology, Imperical College School of Medicine, London, UKSearch for more papers by this author Tessa Carrel, Tessa Carrel Children’s Research Institute and Department of Pediatrics, Ohio State University, Columbus, OhioSearch for more papers by this authorGail E. Herman, Corresponding Author Gail E. Herman [email protected] Children’s Research Institute and Department of Pediatrics, Ohio State University, Columbus, OhioChildren's Research Institute, 700 Children's Dr. Rm. W403, Columbus, OH 43205.Search for more papers by this authorGudrun E. Moore, Gudrun E. Moore Division of Paediatrics, Obsterics, and Gynaecology, Imperical College School of Medicine, London, UKSearch for more papers by this authorPhilip Stanier, Philip Stanier Division of Paediatrics, Obsterics, and Gynaecology, Imperical College School of Medicine, London, UKSearch for more papers by this author First published: 12 January 2001 https://doi.org/10.1002/1096-8628(20010122)98:3<283::AID-AJMG1089>3.0.CO;2-GCitations: 10Read the full textAboutPDF 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 REFERENCES Argua J, Nagai K, Tokuyama Y, Hayashizaki Y, Okazaki Y, Champan VM, Mikoshiba 1996. The mouse zic family. Homologues of the Drosophila pair-rule gene. J Biol Chem 271: 1043– 1047. Baldwin CT, Hoth CF, Macine RA, Milunsky A. 1995. Mutations in PAX3 that cause Waardenburg syndrome type I: ten new mutations and review of the literature. Am J Med Genet 58: 115– 122. Botto LD, Moore CA, Khoury MJ, Erickson JD. 1999. Neural tube defects. New Engl J Med 341: 1509– 1519. Campbell LR, Dayton DH, Sohal GS. 1986. Neural tube defects: a review of human and animal studies on etiology of neural tube defects. Teratol 34: 171– 187. Carrel T, Purandare SM, Harrision W, Elder F, Fox T, Casey B, Herman GE. 2000. The X-linked mouse mutation Bent tail is associated with a deletion of the Zic3 locus. Hum Mol Genet 9: 1937– 1942. Derry JMJ, Gormally E, Means GD, Zhao W, Meindl A, Kelley RI, Body Y, Herman GE. 1999. Mutations in Δ8-Δ7 sterol isomerase in the tattered mouse and X-linked dominant chondroysplasia punctata. Nat Genet 22: 286– 290. Epstein DJ, Vekemans M, Gros P. 1991. Splotch (Sp2H), a mutation affecting development of the mouse neural tube, shows a deletion within the paired homeodomain of Pax-3. Cell 67: 767– 774. Garber ED. 1952. Bent-tail, a dominant, sex-linked mutation in the mouse. Proc Nat Acad Sci USA 38: 876– 879. Gebbia M, Ferrero GB, Pilia G, Bassi MT, Aylsworth A, Penman-Splitt M, Bird LM, Bamforth JS, Burn J, Schlessinger D, Nelson DL, Casey B. 1997. X-linked situs abnormalities resuslt from mutations in ZIC3 Nat Genet 17: 305– 308. Hol FA, Geurds MP, Jensson O, Hamel BC, Moore GE, Newton R, Mariman EC. 1994. Exclusion mapping of the gene for X-linked neural tube defects in an Icelandic family. Hum Genet 93: 452– 456. Hoth CF, Milunsky A, Lipsky J, Sheffer R, Clarren SK, Baldwin CT. 1993. Mutations in the paired domain of the human PAX3 gene cause Klein-Waardenburg (WS-III) as well as Waardenburg syndrome type I (WS-I). Am J Hum Genet 52: 455– 462. Klootwijk R, Franke B, van der Zee CEEM, de Boer RT, Wilms W, Hol FA, Mariman ECM. 2000. A deletion encompassing Zic3 in Bent tail, a mouse model for X-linked neural tube defects. Hum Mol Genet 9: 1615– 1622. Nagai T, Aruga J, Takada S, Gunther T, Sporle R, Schughart K, Mikoshiba K. 1997. The expression of the mouse zicl, zic2 and zic3 genes suggests an essential role for Zic genes in early body pattern formation. Dev Biol 182: 299– 313. Citing Literature Volume98, Issue322 January 2001Pages 283-285 ReferencesRelatedInformation
Publication Year: 2001
Publication Date: 2001-01-01
Language: en
Type: letter
Indexed In: ['crossref', 'pubmed']
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Cited By Count: 13
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