Zobrazeno 1 - 5
of 5
pro vyhledávání: '"P H, Osterberg"'
Autor:
R. A. .B Mollan, Norman C. Nevin, R. J. Barr, A. M. Shearman, J. L. Weber, P. H. Osterberg, Anne E. Hughes, R. G. H. Wallace
Publikováno v:
Human molecular genetics. 3(2)
Familial expansile osteolysis is a rare bone dysplasia which is transmitted as an autosomal dominant trait in a large kindred in Northern Ireland. The gene which causes the disease shows tight linkage with several polymorphic markers on chromosome 18
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d0fcd595668a13b9f1300876a869b13
https://pubmed.ncbi.nlm.nih.gov/7911698
https://pubmed.ncbi.nlm.nih.gov/7911698
Autor:
A. I. Traub, J. A. Weaver, D. Neylan, K. Wilson, D. J. Carson, B. M. Twomey, W. C. J. Collins, J. R. Hayes, H. Kennedy, Hadden, B. Sawhney, T. J. O’hanrahan, A. L. Woods, Vincent DeQuattro, D. Middleton, W. Postlethwaite, L. Kennedy, P. Keenan, M. Murphy, J. D. Baily, D. Brady, Patrick A. Sullivan, B. Magee, J. B. Ferriss, P. P. A. Smyth, S. Sequeira, T. J. McKenna, B. Svheridan, Andrew Foti, B. Sheridan, D. Cregan, Gerald H. Tomkin, P. Skrabanek, R. R. Drury, T. L. Kennedy, R. B. Welbourn, D. J. O’Sullivan, J. A. O’Hare, W. G. Reeves, D. R. Hadden, E. A. Wilson, D. Powell, Noirin Noonan, G. J. Joplin, J. Bain, Michael Hutchinson, J. D. Merrett, M. Byrne, P. H. Osterberg, S. J. Heffernan, A. L. T. Blair, D. K. O’Donovan, P. Dervan, D. A. D. Montgomery, K. Manolas, J. A. Curtis, R. Beacom, W. Thompson, N. M. McMullan, S. M. Kingston, T. J. Lyons, N. McMullan, P. M. Bell, M. I. Drury, J. S. Woodhead, A. B. Atkinson, E. Tempany, D. G. Sinnamon
Publikováno v:
Irish Journal of Medical Science. 153:114-121
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef6c9ebd86271d4886f62cbc47b24493
https://doi.org/10.1007/bf02942004
https://doi.org/10.1007/bf02942004
Autor:
Rab Mollan, D. A. Adams, P. G. Toner, P. H. Osterberg, J. Sloan, G. R. Dickson, R. G. H. Wallace, N. C. Nevin, R. S. Crone, J. A. Kanis
Publikováno v:
The Journal of bone and joint surgery. British volume. 70(2)
We report 40 cases in one family of an autosomal dominant bone dysplasia, which, though similar in some aspects to Paget's disease, seems unique in some features and in its natural history. The disease shows both general and focal skeletal changes, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f41cbac55ef906b7a00b4bb57dc928d7
https://pubmed.ncbi.nlm.nih.gov/3346299
https://pubmed.ncbi.nlm.nih.gov/3346299
Publikováno v:
Clinical orthopaedics and related research. (248)
Familial expansile osteolysis (FEO) is a unique bone dysplasia, which has, over five generations, affected 42 members of a Northern Ireland family. The disease follows a classic autosomal dominant pattern of inheritance. The condition is distinct eno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5db2e83407940d635d26cc207c268fe0
https://pubmed.ncbi.nlm.nih.gov/2530018
https://pubmed.ncbi.nlm.nih.gov/2530018
Publikováno v:
Clinical Orthopaedics and Related Research. 248:265
Familial expansile osteolysis (FEO) is a unique bone dysplasia, which has, over five generations, affected 42 members of a Northern Ireland family. The disease follows a classic autosomal dominant pattern of inheritance. The condition is distinct eno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8761ef2153497272a0efda2d083ea5d
https://doi.org/10.1097/00003086-198911000-00043
https://doi.org/10.1097/00003086-198911000-00043