Conference report: 9th international workshop on fragile X syndrome and X-linked mental retardation

Autor:	Fryns, J.P., Borghgraef, M., Brown, T.W., Chelly, J., Fisch, G.S., Hamel, B.C.J., Hanauer, A., Lacombe, D., Luo, L., MacPherson, J.N., Mandel, J.L., Moraine, C., Mulley, J.C., Nelson, D., Oostra, B.A., Partington, M., Ramakers, G.J., Ropers, H.H., Rousseau, F., Schwartz, C., Steinbach, P., Stoll, C., Tranebjaerg, L., Turner, G., Bokhoven, J.H.L.M. van, Vianna-Morgante, A.M., Villard, L., Warren, S.T.
Rok vydání:	2000
Předmět:	clinical cytogenetic and molecular studies into the relevant gene and their function [X-chromosomal mental retardation (XMR)] klinisch cytogenetisch en moleculair onderzoek naar de betrokken genen en hun functie [X-chromosomale mentale retardatie (XMR)]
Zdroj:	American Journal of Medical Genetics, 94, 345-360 American Journal of Medical Genetics, 94, pp. 345-360
ISSN:	0148-7299
Popis:	Item does not contain fulltext
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::36d822bedcd779d683d69a74c878d1da http://hdl.handle.net/2066/157358 Zobrazit plný text záznamu Plný text