Zobrazeno 1 - 2
of 2
pro vyhledávání: '"MESH: Dwarfism / genetics"'
Autor:
Matthieu P. Robert, Salima El Chehadeh, Geert Vandeweyer, Candace Bensignor, Wilhelmina S. Kerstjens-Frederikse, Darina Prchalova, Hélène Dollfus, Jean-Baptiste Rivière, Christel Thauvin-Robinet, Paul Kuentz, Edwin Reyniers, Patrick Calvas, Caroline Bonnet, Marketa Havlovicova, Rodica Isaiko, Vincent Laugel, Nicolas Chassaing, Julien Thevenon, Christian Gilissen, Morgane Straub, Laurence Faivre, Yannis Duffourd, Miroslava Hancarova, Bart Loeys, R. Frank Kooy, Ange-Line Bruel, Rolph Pfundt, Catherine Creuzot-Garcher, Jolien S. Klein Wassink-Ruiter, Zdenek Sedlacek
Publikováno v:
European Journal of Human Genetics, 25(1), 43-51. Nature Publishing Group
European Journal of Human Genetics, 25, 43-51
European journal of human genetics: EJHG
European journal of human genetics: EJHG, Nature, 2016, 25 (1), pp.43-51. 〈http://www.nature.com/ejhg/index.html〉. 〈10.1038/ejhg.2016.133〉
European Journal of Human Genetics
European Journal of Human Genetics, Nature Publishing Group, 2017, 25 (1), pp.43-51. ⟨10.1038/ejhg.2016.133⟩
European Journal of Human Genetics, Nature Publishing Group, 2016, 25 (1), pp.43-51. ⟨10.1038/ejhg.2016.133⟩
European journal of human genetics
European Journal of Human Genetics, 25, 1, pp. 43-51
European Journal of Human Genetics, 25, 43-51
European journal of human genetics: EJHG
European journal of human genetics: EJHG, Nature, 2016, 25 (1), pp.43-51. 〈http://www.nature.com/ejhg/index.html〉. 〈10.1038/ejhg.2016.133〉
European Journal of Human Genetics
European Journal of Human Genetics, Nature Publishing Group, 2017, 25 (1), pp.43-51. ⟨10.1038/ejhg.2016.133⟩
European Journal of Human Genetics, Nature Publishing Group, 2016, 25 (1), pp.43-51. ⟨10.1038/ejhg.2016.133⟩
European journal of human genetics
European Journal of Human Genetics, 25, 1, pp. 43-51
Item does not contain fulltext Verheij syndrome, also called 8q24.3 microdeletion syndrome, is a rare condition characterized by ante- and postnatal growth retardation, microcephaly, vertebral anomalies, joint laxity/dislocation, developmental delay
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2be171334f26bc8f01ed43d594d5f8c5
https://research.rug.nl/en/publications/daa8a5f7-967c-43ac-87f6-c19664c6accc
https://research.rug.nl/en/publications/daa8a5f7-967c-43ac-87f6-c19664c6accc
Autor:
T. Granier, A. Essautier, Christophe Picard, Agnès Basire, Jacques Chiaroni, Vital Galicher, C. Baier, D. C. Julie, Coralie Frassati, Stéphane Buhler, A. D. Lepfoundzou, A. Regnier
Publikováno v:
Tissue Antigens, Vol. 77, No 3 (2011) pp. 193-200
Tissue Antigens
Tissue Antigens, Wiley, 2011, 77 (3), pp.193-200. ⟨10.1111/j.1399-0039.2010.01599.x.⟩
Tissue Antigens, 2011, 77 (3), pp.193-200. ⟨10.1111/j.1399-0039.2010.01599.x⟩
Tissue Antigens
Tissue Antigens, Wiley, 2011, 77 (3), pp.193-200. ⟨10.1111/j.1399-0039.2010.01599.x.⟩
Tissue Antigens, 2011, 77 (3), pp.193-200. ⟨10.1111/j.1399-0039.2010.01599.x⟩
International audience; Nonclassical human leukocyte antigen (HLA)-G and -E loci are separated by approximately 660 kb on the short arm of chromosome 6. Interestingly, some functional and expression characteristics are relatively identical or associa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbc896fee8bceb19a71c2bfeb1064b77
https://archive-ouverte.unige.ch/unige:14385
https://archive-ouverte.unige.ch/unige:14385