Gray matter heterotopias and brachytelephalangic chondrodysplasia punctata: A complication of hyperemesis gravidarum induced vitamin K deficiency?
2006; Wiley; Volume: 143A; Issue: 2 Linguagem: Inglês
10.1002/ajmg.a.31573
ISSN1552-4833
AutoresNicola Brunetti‐Pierri, Jill V. Hunter, Cornelius F. Boerkoel,
Tópico(s)Drug Transport and Resistance Mechanisms
ResumoAmerican Journal of Medical Genetics Part AVolume 143A, Issue 2 p. 200-204 Research Letter Gray matter heterotopias and brachytelephalangic chondrodysplasia punctata: A complication of hyperemesis gravidarum induced vitamin K deficiency?† Nicola Brunetti-Pierri, Corresponding Author Nicola Brunetti-Pierri [email protected] Departments of Molecular and Human Genetics, Baylor College of Medicine, Houston, TexasBaylor College of Medicine, One Baylor Plaza, Rm 607T, Houston, TX, 77030.Search for more papers by this authorJill V. Hunter, Jill V. Hunter Department of Radiology, Baylor College of Medicine, Houston, TexasSearch for more papers by this authorCornelius F. Boerkoel, Cornelius F. Boerkoel Departments of Molecular and Human Genetics, Baylor College of Medicine, Houston, TexasSearch for more papers by this author Nicola Brunetti-Pierri, Corresponding Author Nicola Brunetti-Pierri [email protected] Departments of Molecular and Human Genetics, Baylor College of Medicine, Houston, TexasBaylor College of Medicine, One Baylor Plaza, Rm 607T, Houston, TX, 77030.Search for more papers by this authorJill V. Hunter, Jill V. Hunter Department of Radiology, Baylor College of Medicine, Houston, TexasSearch for more papers by this authorCornelius F. Boerkoel, Cornelius F. Boerkoel Departments of Molecular and Human Genetics, Baylor College of Medicine, Houston, TexasSearch for more papers by this author First published: 12 December 2006 https://doi.org/10.1002/ajmg.a.31573Citations: 21 † How to cite this article: Brunetti-Pierri N, Hunter JV, Boerkoel CF. 2007. Gray matter heterotopias and brachytelephalangic chondrodysplasia punctata: A complication of hyperemesis gravidarum induced vitamin K deficiency?. Am J Med Genet Part A 143A:200–204. Read 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 onEmailFacebookTwitterLinkedInRedditWechat REFERENCES Austin-Ward E, Castillo S, Cuchacovich M, Espinoza A, Cofre-Beca J, Gonzalez S, Solivelles X, Bloomfield J. 1998. Neonatal lupus syndrome: A case with chondrodysplasia punctata and other unusual manifestations. J Med Genet 35: 695–697. Barkovich AJ, Peck WW. 1997. 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