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Prenatal diagnosis and post-mortem examination in a fetus with thrombocytopenia-absent radius (TAR) syndrome due to compound heterozygosity for a 1q21.1 microdeletion and aRBM8Ahypomorphic allele: a case report

✍ Scribed by Bottillo, Irene; Castori, Marco; De Bernardo, Carmelilia; Fabbri, Romano; Grammatico, Barbara; Preziosi, Nicoletta; Scassellati, Giovanna; Silvestri, Evelina; Spagnuolo, Antonella; Laino, Luigi; Grammatico, Paola


Book ID
121620133
Publisher
BioMed Central
Year
2013
Tongue
English
Weight
510 KB
Volume
6
Category
Article
ISSN
1756-0500

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