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De novo 15q21.1q21.2 deletion identified through FBN1 MLPA ..:
Faivre, Laurence
;
Van Kien, Philippe Khau
;
Callier, Patrick
...
European Journal of Medical Genetics. 53 (2010) 4 - p. 208-212 , 2010
Link:
https://doi.org/10.1016/j.ejmg.2010.05.002
RT Journal T1
De novo 15q21.1q21.2 deletion identified through FBN1 MLPA and refined by 244K array-CGH in a female teenager with incomplete Marfan syndrome
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.ejmg.2010.05.002&Exemplar=1&LAN=DE A1 Faivre, Laurence A1 Van Kien, Philippe Khau A1 Callier, Patrick A1 Ruiz-Pallares, Nathalie A1 Baudoin, Corinne A1 Plancke, Aurélie A1 Wolf, Jean-Eric A1 Thauvin-Robinet, Christel A1 Durand, Edith A1 Minot, Delphine A1 Dulieu, Véronique A1 Metaizeau, Jean-Damien A1 Leheup, Bruno A1 Coron, Fanny A1 Bidot, Samuel A1 Huet, Frédéric A1 Jondeau, Guillaume A1 Boileau, Catherine A1 Claustres, Mireille A1 Mugneret, Francine PB Elsevier BV YR 2010 SN 1769-7212 JF European Journal of Medical Genetics VO 53 IS 4 SP 208 OP 212 LK http://dx.doi.org/https://doi.org/10.1016/j.ejmg.2010.05.002 DO https://doi.org/10.1016/j.ejmg.2010.05.002 SF ELIB - SuUB Bremen
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