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De novo 15q21.1q21.2 deletion identified through FBN1 MLPA and refined by 244K array-CGH in a female teenager with incomplete Marfan syndrome

✍ Scribed by Laurence Faivre; Philippe Khau Van Kien; Patrick Callier; Nathalie Ruiz-Pallares; Corinne Baudoin; Aurélie Plancke; Jean-Eric Wolf; Christel Thauvin-Robinet; Edith Durand; Delphine Minot; Véronique Dulieu; Jean-Damien Metaizeau; Bruno Leheup; Fanny Coron; Samuel Bidot; Frédéric Huet; Guillaume Jondeau; Catherine Boileau; Mireille Claustres; Francine Mugneret


Book ID
116433268
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
614 KB
Volume
53
Category
Article
ISSN
1769-7212

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