-
1دورية أكاديمية
المؤلفون: R. Bertalan, A. Lucas-Herald, Z. Kolesinska, M. Berra, Martine Cools, A. Balsamo, O. Hiort
المصدر: Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-8 (2018)
مصطلحات موضوعية: Differences of sex development network, European Cooperation in Science and Technology, Training school, COST action BM1303, Medicine
وصف الملف: electronic resource
العلاقة: http://link.springer.com/article/10.1186/s13023-018-0967-3Test; https://doaj.org/toc/1750-1172Test
-
2دورية أكاديمية
المؤلفون: K, McElreavey, A, Jorgensen, C, Eozenou, T, Merel, J, Bignon-Topalovic, DS, Tan, D, Houzelstein, F, Buonocore, N, Warr, RGG, Kay, M, Peycelon, JP, Siffroi, I, Mazen, JC, Achermann, Y, Shcherbak, J, Leger, A, Sallai, JC, Carel, L, Martinerie, R, Le Ru, GS, Conway, B, Mignot, L, Van Maldergem, R, Bertalan, E, Globa, R, Brauner, R, Jauch, S, Nef, A, Greenfield, A, Bashamboo
المصدر: Yearbook of Paediatric Endocrinology ; ISSN 1662-4009
الإتاحة: https://doi.org/10.1530/ey.17.6.8Test
http://www.espeyearbook.org/ey/0017/ey0017.6-8.htmTest -
3دورية أكاديمية
المؤلفون: A, Bashamboo, C, Eozenou, A, Jorgensen, J, Bignon-Topalovic, JP, Siffroi, C, Hyon, A, Tar, P, Nagy, J, Sólyom, Z, Halász, A, Paye-Jaouen, S, Lambert, D, Rodriguez-Buritica, R, Bertalan, L, Martinerie, E, Rajpert-De Meyts, JC, Achermann, K, McElreavey
المصدر: Yearbook of Paediatric Endocrinology ; ISSN 1662-4009
الإتاحة: https://doi.org/10.1530/ey.15.6.12Test
http://www.espeyearbook.org/ey/0015/ey0015.6-12.htmTest -
4
المؤلفون: P. Kotnik, K. Poločková, S. Bertok, H.C. Duba, Ľ. Košťálová, R. Bertalan, M. Čizmárová, Z. Pribilincova, László Kovács, Denisa Ilencikova, Katarina Hlinkova, Anna Hlavatá
المصدر: Annals of Human Genetics. 80:50-62
مصطلحات موضوعية: 0301 basic medicine, Genetics, congenital, hereditary, and neonatal diseases and abnormalities, Mutation, Biology, RASopathy, medicine.disease_cause, medicine.disease, Genetic analysis, PTPN11, 03 medical and health sciences, 030104 developmental biology, Genotype, SOS1, medicine, Noonan syndrome, HRAS, skin and connective tissue diseases, Genetics (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::06729c1131a3a664ee655a5e63bf14faTest
https://doi.org/10.1111/ahg.12140Test -
5
-
6
-
7
-
8
-
9
-
10