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Molecular cytogenetic characterization of an 8p22–8p23.2 duplication derived from a maternal intrachromosomal insertion in a child with congenital heart malformation, delayed puberty, and learning disabilities

✍ Scribed by Audrey Basinko; Nathalie Douet-Guilbert; Marie-Josée Le Bris; Philippe Parent; Hélène Ansquer; Frédéric Morel; Marc De Braekeleer


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
179 KB
Volume
146A
Category
Article
ISSN
1552-4825

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