Author:
Baldridge Dustin,Schwarze Ulrike,Morello Roy,Lennington Jennifer,Bertin Terry K.,Pace James M.,Pepin Melanie G.,Weis MaryAnn,Eyre David R.,Walsh Jennifer,Lambert Deborah,Green Andrew,Robinson Haynes,Michelson Melonie,Houge Gunnar,Lindman Carl,Martin Judith,Ward Jewell,Lemyre Emmanuelle,Mitchell John J.,Krakow Deborah,Rimoin David L.,Cohn Daniel H.,Byers Peter H.,Lee Brendan
Subject
Genetics (clinical),Genetics
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3. Cabral WA, Barnes AM, Porter F, Marini JC. 2007a. Carrier frequency of recurring mutation causing severe/lethal recessive type VIII osteogenesis imperfecta in African-Americans. October 23-27, 57th Annual Meeting of the American Society of Human Genetics, San Diego.
4. Prolyl 3-hydroxylase 1 deficiency causes a recessive metabolic bone disorder resembling lethal/severe osteogenesis imperfecta;Cabral;Nat Genet,2007
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