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Osteopathia striata with cranial sclerosis owing to WTX gene defect.
Perdu, Bram; de Freitas, Fenna; Frints, Suzanne G M; Schouten, Meyke; Schrander-Stumpel, Connie; Barbosa, Mafalda; Pinto-Basto, Jorge; Reis-Lima, Margarida; de Vernejoul, Marie-Christine; Becker, Kristin; Freckmann, Marie-Louise; Keymolen, Kathlijn; Haan, Eric; Savarirayan, Ravi; Koenig, Rainer; Zabel, Bernhard; Vanhoenacker, Filip M; Van Hul, Wim.
Affiliation
  • Perdu B; Department of Medical Genetics, University and University Hospital of Antwerp, 2610 Antwerp, Belgium.
J Bone Miner Res ; 25(1): 82-90, 2010 Jan.
Article in En | MEDLINE | ID: mdl-20209645
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skull / Bone Diseases, Developmental / Tumor Suppressor Proteins Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Language: En Journal: J Bone Miner Res Journal subject: METABOLISMO / ORTOPEDIA Year: 2010 Document type: Article Affiliation country: Belgium
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Skull / Bone Diseases, Developmental / Tumor Suppressor Proteins Type of study: Diagnostic_studies / Prognostic_studies Limits: Adolescent / Adult / Aged / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Language: En Journal: J Bone Miner Res Journal subject: METABOLISMO / ORTOPEDIA Year: 2010 Document type: Article Affiliation country: Belgium