Osiris (Egyptian deity) -- Early works to 1800 : Ägyptische Erzählungen oder Über die Vorsehung / Synesios von Kyrene ; herausgegeben von Martin Hose ; eingeleitet, übersetzt und mit interpretierenden Essays versehen von Martin Hose [and others].
2012
1
Abydos (Ägypten) -- Osiristempel. : The great dedicatory inscription of Ramesses II : a Solar-Osirian Tractate at Abydos / by Anthony Spalinger
Oskarshamnsverket (Sweden) / http://id.loc.gov/authorities/subjects/sh2008006820 : Nuclear service water piping : Oskarshamn Nuclear Power Plant, Figeholm, Sweden
1995
1
Oskison, John M. (John Milton), 1874-1947. : Tales of the old Indian territory and essays on the Indian condition / John Milton Oskison ; edited and with an introduction by Lionel Larré
2012
1
Oskison, John M. (John Milton), b. 1874 : Tales of the old Indian territory and essays on the Indian condition / John Milton Oskison ; edited and with an introduction by Lionel Larré
2012
1
Oskolkov, Konstantin Ilyich, 1946- : Recent advances in harmonic analysis and applications : in honor of Konstantin Oskolkov / Dmitriy Bilyk [and others], editors
2013
1
Oskuld -- historia. : Virginity revisited : configurations of the unpossessed body / edited by Bonnie MacLachlan and Judith Fletcher
2007
1
Oskuld i litteraturen. : Virginity revisited : configurations of the unpossessed body / edited by Bonnie MacLachlan and Judith Fletcher
2007
1
Oskuld -- sociala aspekter. : Virginity revisited : configurations of the unpossessed body / edited by Bonnie MacLachlan and Judith Fletcher
2007
1
Oskyldigt dömda. : Conviction of the Innocent : Lessons from Psychological Research / edited by Brian L. Cutler
An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA
An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA
An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA
An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA
An autosomal dominant vascular anomaly characterized by telangiectases of the skin and mucous membranes and by recurrent gastrointestinal bleeding. This disorder is caused by mutations of a gene (on chromosome 9q3) which encodes endoglin, a membrane glycoprotein that binds TRANSFORMING GROWTH FACTOR BETA
