Your browser doesn't support javascript.
loading
Prader-Willi Critical Region, a Non-Translated, Imprinted Central Regulator of Bone Mass: Possible Role in Skeletal Abnormalities in Prader-Willi Syndrome.
Khor, Ee-Cheng; Fanshawe, Bruce; Qi, Yue; Zolotukhin, Sergei; Kulkarni, Rishikesh N; Enriquez, Ronaldo F; Purtell, Louise; Lee, Nicola J; Wee, Natalie K; Croucher, Peter I; Campbell, Lesley; Herzog, Herbert; Baldock, Paul A.
Afiliação
  • Khor EC; Bone and Mineral Research Division, Garvan Institute of Medical Research, Darlinghurst, Sydney, NSW, Australia.
  • Fanshawe B; Bone and Mineral Research Division, Garvan Institute of Medical Research, Darlinghurst, Sydney, NSW, Australia.
  • Qi Y; Neuroscience Division, Garvan Institute of Medical Research, Darlinghurst, Sydney, NSW, Australia.
  • Zolotukhin S; Department of Pediatrics, College of Medicine, Center for Smell and Taste, University of Florida, Gainesville, Florida, United States of America.
  • Kulkarni RN; Bone and Mineral Research Division, Garvan Institute of Medical Research, Darlinghurst, Sydney, NSW, Australia.
  • Enriquez RF; Bone and Mineral Research Division, Garvan Institute of Medical Research, Darlinghurst, Sydney, NSW, Australia.
  • Purtell L; Neuroscience Division, Garvan Institute of Medical Research, Darlinghurst, Sydney, NSW, Australia.
  • Lee NJ; Neuroscience Division, Garvan Institute of Medical Research, Darlinghurst, Sydney, NSW, Australia.
  • Wee NK; School of Medical Sciences, University of NSW, Kensington, Sydney, NSW, Australia.
  • Croucher PI; Bone and Mineral Research Division, Garvan Institute of Medical Research, Darlinghurst, Sydney, NSW, Australia.
  • Campbell L; Bone and Mineral Research Division, Garvan Institute of Medical Research, Darlinghurst, Sydney, NSW, Australia.
  • Herzog H; School of Medical Sciences, University of NSW, Kensington, Sydney, NSW, Australia.
  • Baldock PA; Diabetes and Obesity Research Division, Garvan Institute of Medical Research, Darlinghurst, Sydney, NSW, Australia.
PLoS One ; 11(1): e0148155, 2016.
Article em En | MEDLINE | ID: mdl-26824232

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi / Osso e Ossos / Sequência de Bases / Deleção de Sequência / Impressão Genômica / RNA Nucleolar Pequeno Limite: Animals / Female / Humans / Male Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi / Osso e Ossos / Sequência de Bases / Deleção de Sequência / Impressão Genômica / RNA Nucleolar Pequeno Limite: Animals / Female / Humans / Male Idioma: En Revista: PLoS One Assunto da revista: CIENCIA / MEDICINA Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Austrália