Apolipoprotein B and apolipoprotein E genotypes and sporadic holoprosencephaly
2002; Wiley; Volume: 108; Issue: 1 Linguagem: Inglês
10.1002/ajmg.10134.abs
ISSN1096-8628
AutoresLisa Croen, Gary M. Shaw, Robert C. Barber, Mei M. Baker, Richard H. Finnell, Edward J. Lammer,
Tópico(s)Microtubule and mitosis dynamics
ResumoAmerican Journal of Medical GeneticsVolume 108, Issue 1 p. 75-77 Research Letter Apolipoprotein B and apolipoprotein E genotypes and sporadic holoprosencephaly Lisa A. Croen, Corresponding Author lac@dor.kaiser.org March of Dimes Birth Defects Foundation/California, Department of Health Services California, Birth Defects Monitoring Program, Emeryville, CaliforniaKaiser Permanente, Division of Research, 3505 Broadway, Oakland, California 94611.Search for more papers by this authorGary M. Shaw, March of Dimes Birth Defects Foundation/California, Department of Health Services California, Birth Defects Monitoring Program, Emeryville, CaliforniaSearch for more papers by this authorRobert C. Barber, Department of Pediatrics and Center for Human Molecular Genetics, University of Nebraska Medical Center, Omaha, NebraskaSearch for more papers by this authorMei M. Baker, Department of Pediatrics and Center for Human Molecular Genetics, University of Nebraska Medical Center, Omaha, NebraskaSearch for more papers by this authorRichard H. Finnell, Department of Pediatrics and Center for Human Molecular Genetics, University of Nebraska Medical Center, Omaha, NebraskaSearch for more papers by this authorEdward J. Lammer, Division of Medical Genetics, Children's Hospital Oakland, Oakland, CaliforniaSearch for more papers by this author Lisa A. Croen, Corresponding Author lac@dor.kaiser.org March of Dimes Birth Defects Foundation/California, Department of Health Services California, Birth Defects Monitoring Program, Emeryville, CaliforniaKaiser Permanente, Division of Research, 3505 Broadway, Oakland, California 94611.Search for more papers by this authorGary M. Shaw, March of Dimes Birth Defects Foundation/California, Department of Health Services California, Birth Defects Monitoring Program, Emeryville, CaliforniaSearch for more papers by this authorRobert C. Barber, Department of Pediatrics and Center for Human Molecular Genetics, University of Nebraska Medical Center, Omaha, NebraskaSearch for more papers by this authorMei M. Baker, Department of Pediatrics and Center for Human Molecular Genetics, University of Nebraska Medical Center, Omaha, NebraskaSearch for more papers by this authorRichard H. Finnell, Department of Pediatrics and Center for Human Molecular Genetics, University of Nebraska Medical Center, Omaha, NebraskaSearch for more papers by this authorEdward J. Lammer, Division of Medical Genetics, Children's Hospital Oakland, Oakland, CaliforniaSearch for more papers by this author First published: 16 January 2002 https://doi.org/10.1002/ajmg.10134Citations: 2Read 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 Share a linkShare onEmailFacebookTwitterLinked InRedditWechat No abstract is available for this article.Citing Literature Volume108, Issue115 February 2002Pages 75-77 RelatedInformation
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