The male phenotype in osteopathia striata congenita with cranial sclerosis.

Holman, Sarah K; Daniel, Phil; Jenkins, Zandra A; Herron, Rachel L; Morgan, Tim; Savarirayan, Ravi; Chow, C W; Bohring, Axel; Mosel, Annette; Lacombe, Didier; Steiner, Bernhard; Schmitt-Mechelke, Thomas; Schroter, Barbara; Raas-Rothschild, Annick; Miñaur, Sixto Garcia; Porteous, Mary; Parker, Michael; Quarrell, Oliver; Tapon, Dagmar; Cormier-Daire, Valérie; Mansour, Sahar; Nash, Ruth; Bindoff, Laurence A; Fiskerstrand, Torunn; Robertson, Stephen P

Holman, Sarah K; Daniel, Phil; Jenkins, Zandra A; Herron, Rachel L; Morgan, Tim; Savarirayan, Ravi; Chow, C W; Bohring, Axel; Mosel, Annette; Lacombe, Didier; Steiner, Bernhard; Schmitt-Mechelke, Thomas; Schroter, Barbara; Raas-Rothschild, Annick; Miñaur, Sixto Garcia; Porteous, Mary; Parker, Michael; Quarrell, Oliver; Tapon, Dagmar; Cormier-Daire, Valérie; Mansour, Sahar; Nash, Ruth; Bindoff, Laurence A; Fiskerstrand, Torunn; Robertson, Stephen P.

Affiliation

Holman SK; Department of Paediatrics, Dunedin School of Medicine, Otago University, New Zealand.

Am J Med Genet A ; 155A(10): 2397-408, 2011 Oct.

Article de En | MEDLINE | ID: mdl-22043478

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Collection: 01-internacional Base de données: MEDLINE Sujet principal: Ostéosclérose / Phénotype / Maladies génétiques liées au chromosome X Limites: Female / Humans / Male Langue: En Journal: Am J Med Genet A Sujet du journal: GENETICA MEDICA Année: 2011 Type de document: Article Pays d'affiliation: Nouvelle-Zélande

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