Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly
1989; Wiley; Volume: 34; Issue: 2 Linguagem: Inglês
10.1002/ajmg.1320340222
ISSN1096-8628
Autores Tópico(s)Epigenetics and DNA Methylation
ResumoAmerican Journal of Medical GeneticsVolume 34, Issue 2 p. 237-245 Invited Editorial Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly Dr. Maximilian Münke, Corresponding Author Dr. Maximilian Münke Howard Hughes Medical Institute and Department of Human Genetics, University of Pennsylvania School of Medicine and Division of Human Genetics and Molecular Biology, The Children's Hospital of Philadelphia, PhiladelphiaDepartment of Human Genetics, University of Pennsylvania School of Medicine, 37th and Hamilton Walk, Philadelphia, PA 19104–6072Search for more papers by this author Dr. Maximilian Münke, Corresponding Author Dr. Maximilian Münke Howard Hughes Medical Institute and Department of Human Genetics, University of Pennsylvania School of Medicine and Division of Human Genetics and Molecular Biology, The Children's Hospital of Philadelphia, PhiladelphiaDepartment of Human Genetics, University of Pennsylvania School of Medicine, 37th and Hamilton Walk, Philadelphia, PA 19104–6072Search for more papers by this author First published: October 1989 https://doi.org/10.1002/ajmg.1320340222Citations: 81AboutPDF 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. 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