Zobrazeno 1 - 8
of 8
pro vyhledávání: '"R D, Blank"'
Autor:
R D, Blank
Publikováno v:
Journal of clinical densitometry : the official journal of the International Society for Clinical Densitometry. 2(1)
Most medical genetic studies seek to answer one of two questions: What genes are important in determining disease risk? and What alleles of a candidate gene confer excess risk? This article seeks to provide physicians with a practical approach to ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c5cf7b16da138858708810680637b301
https://pubmed.ncbi.nlm.nih.gov/23547315
https://pubmed.ncbi.nlm.nih.gov/23547315
Autor:
P F, Giampietro, C L, Raggio, C E, Reynolds, S K, Shukla, E, McPherson, N, Ghebranious, F S, Jacobsen, V, Kumar, T, Faciszewski, R M, Pauli, K, Rasmussen, J K, Burmester, C, Zaleski, S, Merchant, D, David, J L, Weber, I, Glurich, R D, Blank
Publikováno v:
Clinical genetics. 68(5)
An analysis of PAX1 in the development of vertebral malformations. Due to the sporadic occurrence of congenital vertebral malformations, traditional linkage approaches to identify genes associated with human vertebral development are not possible. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::eda8eec266525a0363d6d6dc55339d1e
https://pubmed.ncbi.nlm.nih.gov/16207213
https://pubmed.ncbi.nlm.nih.gov/16207213
Publikováno v:
American journal of medical genetics. 83(3)
Idiopathic scoliosis (IS) is a common but poorly understood syndrome. Congenital scoliosis (CS) is less common but comparably unexplored. Previous studies suggest that each has a significant genetic component. However, the occurrence of scoliosis in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a10992c59ddf443f87df9a1ba1377ddb
https://pubmed.ncbi.nlm.nih.gov/10096591
https://pubmed.ncbi.nlm.nih.gov/10096591
Publikováno v:
Cancer. 78(9)
Multiple endocrine neoplasia type 2 (MEN 2) is a group of related autosomal dominant cancer syndromes caused by mutations in the RET protooncogene. A subset of familial Hirschsprung's disease, aganglionic megacolon, is also caused by mutations in thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::581bf9c96957786053a5347dd20778ec
https://pubmed.ncbi.nlm.nih.gov/8909322
https://pubmed.ncbi.nlm.nih.gov/8909322
Autor:
E. ühlein, W. Schermann, H. SchÄfer, R. D. Blank, H. K. Kugler, E. Best, H. H. Pfeiffer, P. Kratochvíl, P. Zuman, R. Keim, C. Mahr
Publikováno v:
Kolloid-Zeitschrift & Zeitschrift für Polymere. 212:170-177
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b3d2094f6e4611cd17f80e68be2abcb3
https://doi.org/10.1007/bf01553089
https://doi.org/10.1007/bf01553089
Autor:
E. Gruner, H. Kübler, W. Schanzer, W. Schermann, A. Warner, F. Bohlmann, B. Schrader, K. Heyns, H. Kienitz, R. D. Blank, H. Bergmann, E. ühlein, K. Koeber, G. Kirschstein, A. Giller, G. Ebert, J. Volke, K. Wellinger, H. H. Pfeiffer, H. Siebert, R. Jaenicke, F. Schneider, H. Sucker, R. Haase, F. Prinzhorn
Publikováno v:
Kolloid-Zeitschrift und Zeitschrift für Polymere. 218:63-78
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac157825f778a10848f26f38c2c6981e
https://doi.org/10.1007/bf01517281
https://doi.org/10.1007/bf01517281
Autor:
E. Ühlein, R. D. Blank, H. H. Pfeiffer, H. Schäfer, H. Bergmann, P. Kratochvíl, A. Sippel, R. Hähnel, E. Best
Publikováno v:
Kolloid-Zeitschrift & Zeitschrift für Polymere. 219:52-96
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::193d6f5ac59622b7fa31c9728a83d061
https://doi.org/10.1007/bf02086097
https://doi.org/10.1007/bf02086097
Autor:
R D, Blank
Publikováno v:
Dental clinics of North America. 25(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::67646c3ab8f3ee870b5866ccb72f496f
https://pubmed.ncbi.nlm.nih.gov/6943103
https://pubmed.ncbi.nlm.nih.gov/6943103