Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

A Genotypic and Histopathological Study of a Large Dutch Kindred with Hyperparathyroidism-Jaw Tumor Syndrome

Autor: Haven, Carola Jose, Wong, Fung Ki, Van Dam, Eveline W.C.M., Van Der Luijt, Rob, Van Asperen, Christi, Jansen, Joke, Rosenberg, Carla, De Wit, Mireille, Roijers, Janine, Hoppener, Jo, Lips, Cornelis J., Larsson, Catharina, Teh, Bin Tean, Morreau, Hans

Publikováno v: Journal of Clinical Endocrinology and Metabolism, 85(4), 1449-1454. The Endocrine Society
Haven, C J, Wong, F K, Van Dam, E W C M, Van Der Luijt, R, Van Asperen, C, Jansen, J, Rosenberg, C, De Wit, M, Roijers, J, Hoppener, J, Lips, C J, Larsson, C, Teh, B T & Morreau, H 2000, ' A genotypic and histopathological study of a large Dutch kindred with hyperparathyroidism-jaw tumor syndrome ', Journal of Clinical Endocrinology and Metabolism, vol. 85, no. 4, pp. 1449-1454 . https://doi.org/10.1210/jc.85.4.1449

Familial primary hyperparathyroidism is the main feature of 2 familial endocrine neoplasia syndromes: multiple endocrine neoplasia type 1 (MEN 1) and hyperparathyroidism-jaw tumor syndrome (HPT-JT). The latter is a recently described syndrome that ha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d184b037a782cdc62a71207716a2ca4d
https://doi.org/10.1210/jc.85.4.1449

Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.

Molecular evidence for the same clonal origin of both components of an adenosquamous barrett carcinoma

Autor: van Rees, Bastiaan P., Rouse, Remigio W., De Wit, Mireille J., van Noesel, Carel J.M., Tytgat, Guido N.J., van Lanschot, J. Jan B., Offerhaus, G. Johan A.

Publikováno v: In Gastroenterology March 2002 122(3):784-788

Construction of a 1.2-Mb Sequence-Ready Contig of Chromosome 11q13 Encompassing the Multiple Endocrine Neoplasia Type 1 (MEN1) Gene

Autor: Lemmens, Irma, Merregaert, Jozef, Van de Ven, Wim J.M., Kas, Koen, Zhang, Chang X., Giraud, Sophie, Wautot, Virginie, Buisson, Nathalie, De Witte, Ko, Salandre, Janine, Lenoir, Gilbert, Calender, Alain, Parente, Fabienne, Quincey, Danielle, Courseaux, Anouk, Carle, George F., Gaudray, Patrick, De Wit, Mireille J., Lips, Cornelis J.M., Höppener, Jo W.M., Khodaei, Shideh, Grant, Abby L., Weber, Günther, Kytölä, Soili, Teh, Bin T., Farnebo, Filip, Grimmond, Sean, Phelan, Catherine, Larsson, Catharina, Forbes, Simon A., Bassett, J.H.Duncan, Pannett, Anna A.J., Thakker, Rajesh V.

Publikováno v: Genomics; August 1997, Vol. 44 Issue: 1 p94-100, 7p