SHOX point mutations and deletions in Leri-Weill dyschondrosteosis

Saved in:

Bibliographic Details
Published in:	Journal of medical genetics Vol. 39; no. 6; pp. e33 - 33
Main Authors:	Falcinelli, C, Iughetti, L, Percesepe, A, Calabrese, G, Chiarelli, F, Cisternino, M, De Sanctis, L, Pucarelli, I, Radetti, G, Wasniewska, M, Weber, G, Stuppia, L, Bernasconi, S, Forabosco, A
Format:	Journal Article
Language:	English
Published:	England BMJ Publishing Group Ltd 01-06-2002 BMJ Publishing Group LTD BMJ Group
Subjects:	Adolescent Child Child, Preschool DNA Mutational Analysis Family Health Female Gene Deletion Homeodomain Proteins - genetics Humans Infant Italy Leri-Weill dyschondrosteosis Male Mutation Online Mutation Report Osteochondrodysplasias - diagnosis Osteochondrodysplasias - genetics Point Mutation Short Stature Homeobox Protein SHOX point mutations Italy
Online Access:	Get full text
Tags:	Add Tag No Tags, Be the first to tag this record!

Description
Bibliography:	local:03900e33 href:jmedgenet-39-e33.pdf PMID:12070265 Correspondence to:  Dr A Forabosco, Cattedra di Genetica Medica, Università di Modena, Via del Pozzo 71, 41100 Modena, Italy;  forabosco.antonino@unimo.it ark:/67375/NVC-52NL87VR-F istex:88D6A35796B64B28D94A494119FCF93F9C7E3A15 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23
ISSN:	0022-2593 1468-6244 1468-6244
DOI:	10.1136/jmg.39.6.e33