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• W1566530004 abstract "Clinical GeneticsVolume 69, Issue 4 p. 367-369 Identification of a submicroscopic deletion of SHH associated with the holoprosencephaly spectrum by array-based CGH Jia Huang, Jia Huang Abramson Family Cancer Research Institute, The University of Pennsylvania, Philadelphia, PA, USA, andSearch for more papers by this authorJodi D. Hoffman, Jodi D. Hoffman Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia and The University of Pennsylvania School of Medicine, Philadelphia, PA, USASearch for more papers by this authorYi Zhang, Yi Zhang Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia and The University of Pennsylvania School of Medicine, Philadelphia, PA, USASearch for more papers by this authorMelissa K. Maisenbacher, Melissa K. Maisenbacher Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia and The University of Pennsylvania School of Medicine, Philadelphia, PA, USASearch for more papers by this authorElaine H. Zackai, Elaine H. Zackai Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia and The University of Pennsylvania School of Medicine, Philadelphia, PA, USASearch for more papers by this authorBarbara L. Weber, Barbara L. Weber Abramson Family Cancer Research Institute, The University of Pennsylvania, Philadelphia, PA, USA, andSearch for more papers by this authorJeffrey E. Ming, Corresponding Author Jeffrey E. Ming Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia and The University of Pennsylvania School of Medicine, Philadelphia, PA, USA Jeffrey E. Ming, MD, PhD The Children's Hospital of Philadelphia Abramson Research Building, Room 1002 3615 Civic Center Boulevard PA 19104, USA e-mail: jeming@mail.med.upenn.eduTel.: +1 215 590 3856 Fax: +1 215 590 3764Search for more papers by this author Jia Huang, Jia Huang Abramson Family Cancer Research Institute, The University of Pennsylvania, Philadelphia, PA, USA, andSearch for more papers by this authorJodi D. Hoffman, Jodi D. Hoffman Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia and The University of Pennsylvania School of Medicine, Philadelphia, PA, USASearch for more papers by this authorYi Zhang, Yi Zhang Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia and The University of Pennsylvania School of Medicine, Philadelphia, PA, USASearch for more papers by this authorMelissa K. Maisenbacher, Melissa K. Maisenbacher Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia and The University of Pennsylvania School of Medicine, Philadelphia, PA, USASearch for more papers by this authorElaine H. Zackai, Elaine H. Zackai Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia and The University of Pennsylvania School of Medicine, Philadelphia, PA, USASearch for more papers by this authorBarbara L. Weber, Barbara L. Weber Abramson Family Cancer Research Institute, The University of Pennsylvania, Philadelphia, PA, USA, andSearch for more papers by this authorJeffrey E. Ming, Corresponding Author Jeffrey E. Ming Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia and The University of Pennsylvania School of Medicine, Philadelphia, PA, USA Jeffrey E. Ming, MD, PhD The Children's Hospital of Philadelphia Abramson Research Building, Room 1002 3615 Civic Center Boulevard PA 19104, USA e-mail: jeming@mail.med.upenn.eduTel.: +1 215 590 3856 Fax: +1 215 590 3764Search for more papers by this author First published: 30 March 2006 https://doi.org/10.1111/j.1399-0004.2006.00598.xCitations: 1Read 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 onFacebookTwitterLinked InRedditWechat Citing Literature Volume69, Issue4April 2006Pages 367-369 RelatedInformation" @default.
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• W1566530004 title "Identification of a submicroscopic deletion of SHH associated with the holoprosencephaly spectrum by array-based CGH" @default.
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