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Genética
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Exome Sequencing Identifies Truncating Mutations in Human
SERPINF1 in Autosomal-Recessive Osteogenesis Imperfecta.
Jutta Becker, Oliver Semler y
col. 2011
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Mutations in SERPINF1 Cause Osteogenesis Imperfecta
Type VI. Erica P. Homan, Frank Rauch, y col. 2011
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Osteogenesis imperfecta type VI in childhood and
adolescence: Effects of cyclical intravenous pamidronate
treatment. Christof Land, Frank Rauch, Rose Travers,
Francis H. Glorieux. 2007
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Un futuro sin
enfermedades genéticas. Glenys Álvarez. 2004
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Osteogenesis Imperfecta Type VI: A Form of Brittle Bone
Disease with a Mineralization Defect. Francis H.
Glorieux, Leanne M. Ward, Frank Rauch, Liliana Lalic, Peter
J Roughley and Rose Travers. 2002
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Metodología
de asesoramiento genético postnatal en la OI tipo I.
Yolaysi Comendador Zamora. 2002.
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Mutations in type I
collagen genes resulting in osteogenesis imperfecta in humans.
Anna Gajko-Galicka.
Enlace
al documento original. 2002
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The Bone Builders.
Scientists are developing stem cell and gene therapies to repair
fractures and treat bone loss.
Bijal
P. Trivedi.
Enlace
al documento original. 2001
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MOLECULAR APPROACH FOR
THE IDENTIFICATION OF THE UNDERLYING MUTATION IN PATIENTS WITH
OSTEOGENESIS IMPERFECTA TYPE I. L. Nuytinck, K. Wettinck,
M. Van Thielen, A. De Paepe.
Enlace
al documento original. 1999
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Correo electrónico: contacto@osteogenesis.info
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