Abstract
American Journal of Medical GeneticsVolume 106, Issue 4 p. 241-243 Introduction Latest developments in skeletal dysplasias# Nicola C. Ho, Nicola C. Ho Guest Editor Nicola C. Ho is a pediatrician and medical geneticist. She is Assistant Professor of Pediatrics at Johns Hopkins University School of Medicine, and a research scientist with the National Institutes of Health. Dr. Ho's interests include dysmorphology, skeletal dysplasias, connective tissue disorders, molecular genetics, and study of genetic disorders in inbred populations.Search for more papers by this authorClair A. Francomano, Corresponding Author Clair A. Francomano Guest Editor francomanocl@grc.nia.nih.gov Section of Human Genetics and Integrative Medicine, Laboratory of Genetics, NIA/NIH-IRP, Room 4A, 5600 Nathan Shock Drive, Baltimore, MD 21224-6825. Clair Francomano is an internist and medical geneticist whose work has centered on the hereditary connective tissue disorders and skeletal dysplasias. She has published widely on the molecular genetics underlying human connective tissue disorders and skeletal dysplasias. She serves on the Advisory Boards for the National Marfan Foundation and the Little People of America. Her current position is Senior Investigator, Laboratory of Genetics, National Institute on Aging.Section of Human Genetics and Integrative Medicine, Laboratory of Genetics, NIA/NIH-IRP, Room 4A, 5600 Nathan Shock Drive, Baltimore, MD 21224-6825.Search for more papers by this author Nicola C. Ho, Nicola C. Ho Guest Editor Nicola C. Ho is a pediatrician and medical geneticist. She is Assistant Professor of Pediatrics at Johns Hopkins University School of Medicine, and a research scientist with the National Institutes of Health. Dr. Ho's interests include dysmorphology, skeletal dysplasias, connective tissue disorders, molecular genetics, and study of genetic disorders in inbred populations.Search for more papers by this authorClair A. Francomano, Corresponding Author Clair A. Francomano Guest Editor francomanocl@grc.nia.nih.gov Section of Human Genetics and Integrative Medicine, Laboratory of Genetics, NIA/NIH-IRP, Room 4A, 5600 Nathan Shock Drive, Baltimore, MD 21224-6825. Clair Francomano is an internist and medical geneticist whose work has centered on the hereditary connective tissue disorders and skeletal dysplasias. She has published widely on the molecular genetics underlying human connective tissue disorders and skeletal dysplasias. She serves on the Advisory Boards for the National Marfan Foundation and the Little People of America. Her current position is Senior Investigator, Laboratory of Genetics, National Institute on Aging.Section of Human Genetics and Integrative Medicine, Laboratory of Genetics, NIA/NIH-IRP, Room 4A, 5600 Nathan Shock Drive, Baltimore, MD 21224-6825.Search for more papers by this author First published: 23 October 2002 https://doi.org/10.1002/ajmg.10232 # This article is a US Government work and, as such, is in the public domain in the United States of America. 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 onFacebookTwitterLinkedInRedditWechat No abstract is available for this article. Volume106, Issue4Special Issue: Latest Developments in Skeletal DysplasiasWinter 2001Pages 241-243 RelatedInformation
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