Mutations in WNT1 cause different forms of bone fragility.

WOLLNIK, B; Altunoglu, UMUT; SCHÖNAU, E; RUIZ-PEREZ, VL; MUNDLOS, S; AMLING, M; KORNAK, U; MARINI, J; KEUPP, K; YIGIT, Günnur; KAYSERILI, H; BELEGGIA, F; BARNES, AM; STEINER, M; SEMLER, O; FISCHER, B; JANDA, CY; BECKER, J; BREER, S; GRÜNHAGEN, J; KRAWITZ, P; HECHT, J; SCHINKE, T; MAKAREEVA, E; LAUSCH, E; CANKAYA, T; CAPARRÓS-MARTÍN, JA; LAPUNZINA, P; TEMTAMY, S; AGLAN, M; ZABEL, B; EYSEL, P; KOERBER, F; LEIKIN, S; GARCIA, KC; NETZER, C

dc.contributor.author	WOLLNIK, B
dc.contributor.author	Altunoglu, UMUT
dc.contributor.author	SCHÖNAU, E
dc.contributor.author	RUIZ-PEREZ, VL
dc.contributor.author	MUNDLOS, S
dc.contributor.author	AMLING, M
dc.contributor.author	KORNAK, U
dc.contributor.author	MARINI, J
dc.contributor.author	KEUPP, K
dc.contributor.author	YIGIT, Günnur
dc.contributor.author	KAYSERILI, H
dc.contributor.author	BELEGGIA, F
dc.contributor.author	BARNES, AM
dc.contributor.author	STEINER, M
dc.contributor.author	SEMLER, O
dc.contributor.author	FISCHER, B
dc.contributor.author	JANDA, CY
dc.contributor.author	BECKER, J
dc.contributor.author	BREER, S
dc.contributor.author	GRÜNHAGEN, J
dc.contributor.author	KRAWITZ, P
dc.contributor.author	HECHT, J
dc.contributor.author	SCHINKE, T
dc.contributor.author	MAKAREEVA, E
dc.contributor.author	LAUSCH, E
dc.contributor.author	CANKAYA, T
dc.contributor.author	CAPARRÓS-MARTÍN, JA
dc.contributor.author	LAPUNZINA, P
dc.contributor.author	TEMTAMY, S
dc.contributor.author	AGLAN, M
dc.contributor.author	ZABEL, B
dc.contributor.author	EYSEL, P
dc.contributor.author	KOERBER, F
dc.contributor.author	LEIKIN, S
dc.contributor.author	GARCIA, KC
dc.contributor.author	NETZER, C
dc.date.accessioned	2021-03-05T18:59:49Z
dc.date.available	2021-03-05T18:59:49Z
dc.identifier.citation	KEUPP K., BELEGGIA F., KAYSERILI H., BARNES A., STEINER M., SEMLER O., FISCHER B., YIGIT G., JANDA C., BECKER J., et al., "Mutations in WNT1 cause different forms of bone fragility.", American journal of human genetics, cilt.92, ss.565-74, 2013
dc.identifier.issn	0002-9297
dc.identifier.other	vv_1032021
dc.identifier.other	av_cd182f71-b0d7-45d8-aac7-b1efd80130a3
dc.identifier.uri	http://hdl.handle.net/20.500.12627/135748
dc.identifier.uri	https://doi.org/10.1016/j.ajhg.2013.02.010
dc.language.iso	eng
dc.title	Mutations in WNT1 cause different forms of bone fragility.
dc.type	Makale
dc.relation.journal	American journal of human genetics
dc.contributor.department	, ,
dc.identifier.volume	92
dc.identifier.startpage	565
dc.identifier.endpage	74
dc.contributor.firstauthorID	181846

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