Zobrazeno 1 - 10
of 2 029
pro vyhledávání: '"Levilliers, J"'
Autor:
Zhou, Lin1 (AUTHOR), Peng, Ying1 (AUTHOR), Chen, Jing1 (AUTHOR), Xi, Hui1 (AUTHOR), Wang, Si1 (AUTHOR), Kang, Gehua2 (AUTHOR), Tang, Wanglan1 (AUTHOR), Xie, Wanqin3 (AUTHOR) wanqinxie@126.com
Publikováno v:
BMC Medical Genomics. 10/18/2024, Vol. 17 Issue 1, p1-7. 7p.
Autor:
Lattanzi, Roberta1 (AUTHOR) roberta.lattanzi@uniroma1.it, Miele, Rossella2 (AUTHOR) roberta.lattanzi@uniroma1.it
Publikováno v:
Life (2075-1729). Oct2024, Vol. 14 Issue 10, p1254. 16p.
Publikováno v:
Advances in Oto-Rhino-Laryngology; 2000, Vol. 56, p268-274, 7p
Autor:
Jung, Joonho1 (AUTHOR) jhjung95@yuhs.ac, Jang, Seung Hyun1,2 (AUTHOR) hygee@yuhs.ac, Won, Dongju3 (AUTHOR) wdjbabo@yuhs.ac, Gee, Heon Yung2 (AUTHOR), Choi, Jae Young1 (AUTHOR) jychoi@yuhs.ac, Jung, Jinsei1 (AUTHOR) jsjung@yuhs.ac
Publikováno v:
Journal of Clinical Medicine. Aug2024, Vol. 13 Issue 16, p4851. 11p.
Autor:
Zouaghi, Yassine1,2 (AUTHOR), Choudhary, Anbreen Mazhar3,4 (AUTHOR), Irshad, Saba3 (AUTHOR), Adamo, Michela1,2 (AUTHOR), Rehman, Khaleeq ur4 (AUTHOR), Fatima, Ambrin5 (AUTHOR), Shahid, Mariam6 (AUTHOR), Najmi, Nida7 (AUTHOR), De Azevedo Correa, Fernanda1,2 (AUTHOR), Habibi, Imen1,2 (AUTHOR), Boizot, Alexia1,2 (AUTHOR), Niederländer, Nicolas J.1,2 (AUTHOR), Ansar, Muhammad8,9 (AUTHOR), Santoni, Federico1,2,10 (AUTHOR), Acierno, James2 (AUTHOR), Pitteloud, Nelly1,2 (AUTHOR) nelly.pitteloud@chuv.ch
Publikováno v:
BMC Genomics. 8/14/2024, Vol. 25 Issue 1, p1-9. 9p.
Autor:
Chan Jong Yu1 (AUTHOR) cjyu@kangwon.ac.kr, Yoon Ho Park1 (AUTHOR) yhpark99@kangwon.ac.kr, Mi Young An1 (AUTHOR), Bumhan Ryu2 (AUTHOR), Hyun Suk Jung1 (AUTHOR) hsjung@kangwon.ac.kr
Publikováno v:
Molecules. Jul2024, Vol. 29 Issue 13, p1-13. 13p. 5 Color Photographs.
Autor:
Hardelin, J. P., nadia Soussi-Yanicostas, Levilliers, J., Kalatzis, V., Abdelhak, S., Cohen-Salmon, M., Petit, C.
Publikováno v:
Europe PubMed Central
Scopus-Elsevier
Scopus-Elsevier
Publikováno v:
Advances in Oto-Rhino-Laryngology; 2000, Vol. 56, p78-83, 6p
Autor:
Well, D., Blanchard, S., Kaplan, J., Guilford, P., Gibson, F., Walsh, J., Mburu, P., Varela, A., Levilliers, J., Weston, M.D., Kelley, P.M., Kimberling, W.J., Wagenaar, M., Levi-Acobas, F., Larget-Piet, D., Munnich, A., Steel, K.P., Brown, S.D.M., Petit, C.
Publikováno v:
Nature, 374, 6517, pp. 60-61
Nature, 374, 60-61
Nature, 374, pp. 60-61
Nature, 374, 60-61
Nature, 374, pp. 60-61
Contains fulltext : 22411___.PDF (Publisher’s version ) (Open Access)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::155471e6f7d258fbb6e2ee7641c6bf73
https://hdl.handle.net/2066/22411
https://hdl.handle.net/2066/22411
Autor:
Thomas Meitinger, Heye, B., Petit, C., Levilliers, J., Golla, A., Moraine, C., Dalla Piccola, B., Sippell, W. G., Murken, J., Ballabio, A.
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Kallmann syndrome is a genetically heterogeneous disease characterized by hypogonadotropic hypogonadism and anosmia. Six families in which the disorder followed an X-linked inheritance were investigated by linkage analysis. Diagnostic criteria were u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::639fa2d3b04b6379c0a858fc8ce9c277
https://europepmc.org/articles/PMC1683776/
https://europepmc.org/articles/PMC1683776/