Zobrazeno 1 - 10
of 706
pro vyhledávání: '"J. Grosfeld"'
Autor:
Douglas, Lawrence (AUTHOR) lrdouglas@amherst.edu
Publikováno v:
Bulletin of the Atomic Scientists. Sep2024, Vol. 80 Issue 5, p287-290. 4p.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
De Rydt, Jan1 (AUTHOR) jan.rydt@northumbria.ac.uk, Jourdain, Nicolas C.2 (AUTHOR), Nakayama, Yoshihiro3 (AUTHOR), van Caspel, Mathias4 (AUTHOR), Timmermann, Ralph4 (AUTHOR), Mathiot, Pierre2 (AUTHOR), Asay-Davis, Xylar S.5 (AUTHOR), Seroussi, Hélène6 (AUTHOR), Dutrieux, Pierre7 (AUTHOR), Galton-Fenzi, Ben8 (AUTHOR), Holland, David9 (AUTHOR), Reese, Ronja1 (AUTHOR)
Publikováno v:
Geoscientific Model Development. 2024, Vol. 17 Issue 18, p7105-7139. 35p.
Autor:
ARPIGIANI, DANIELA1,2 dfarpigiani@unrn.edu.ar, CHILLO, VERÓNICA3, SOLER, ROSINA4, AMOROSO, MARIANO M.1,2
Publikováno v:
Ecologia Austral. Aug2024, Vol. 34 Issue 2, p213-227. 15p.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
American journal of medical genetics. 94(4)
The psychological reactions of 22 parental couples and 3 single parents were investigated after disclosure of genetic test results of their children. The children were tested for the early-onset, monogenetic cancer disorder multiple endocrine neoplas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6a67074b431b2038c9524893cb4a5e75
https://pubmed.ncbi.nlm.nih.gov/11038446
https://pubmed.ncbi.nlm.nih.gov/11038446
Autor:
H F, ten Kroode, I M, van Langen, K S, Hendriks, J P, van Tintelen, F J, Grosfeld, A A, Wilde
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 144(21)
DNA diagnostics were carried out in a family after the long QT interval syndrome had been diagnosed in one of its members. The psychic reactions to this testing were different from those seen in other hereditary diseases such as Huntington's disease.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f1308a4ce7fa4fda64d55ca88521de9d
https://pubmed.ncbi.nlm.nih.gov/10858789
https://pubmed.ncbi.nlm.nih.gov/10858789
Autor:
F J, Grosfeld, C J, Lips, F A, Beemer, G H, Blijham, J M, Quirijnen, M P, Mastenbroek, H F, ten Kroode
Publikováno v:
American journal of medical genetics. 91(1)
Multiple endocrine neoplasia type 2 (MEN 2) is an autosomal dominant early-onset cancer disorder. In the Netherlands presymptomatic genetic testing for MEN 2 is offered to testees from the age of five years. We report on adults requesting testing for
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bd6fff14fb7b0bec06baa21a1f48b342
https://pubmed.ncbi.nlm.nih.gov/10751081
https://pubmed.ncbi.nlm.nih.gov/10751081
Autor:
Hoffman, Matthew J.1 (AUTHOR) mhoffman@lanl.gov, Branecky Begeman, Carolyn1 (AUTHOR), Asay-Davis, Xylar S.1 (AUTHOR), Comeau, Darin1 (AUTHOR), Barthel, Alice1 (AUTHOR), Price, Stephen F.1 (AUTHOR), Wolfe, Jonathan D.1 (AUTHOR)
Publikováno v:
Cryosphere. 2024, Vol. 18 Issue 6, p2917-2937. 21p.
Autor:
Matteucci, Andrea1,2 (AUTHOR) andrea.matteucci2@gmail.com, Pignalberi, Carlo1 (AUTHOR), Pandozi, Claudio1 (AUTHOR), Magris, Barbara1 (AUTHOR), Meo, Antonella1 (AUTHOR), Russo, Maurizio1 (AUTHOR), Galeazzi, Marco1 (AUTHOR), Schiaffini, Giammarco1 (AUTHOR), Aquilani, Stefano1 (AUTHOR), Di Fusco, Stefania Angela1 (AUTHOR), Colivicchi, Furio1 (AUTHOR)
Publikováno v:
Journal of Clinical Medicine. May2024, Vol. 13 Issue 9, p2707. 14p.