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Clinical evaluation and COL2A1 gene analysis in 21 Brazilian families with Stickler syndrome: Identification of novel mutations, further genotype/phenotype correlation, and its implications for the diagnosis

✍ Scribed by Roseli Maria Zechi-Ceide; Nélio Alessando Jesus Oliveira; Maria Leine Guion-Almeida; Luís Fernando B.B. Antunes; Antonio Richieri-Costa; Maria Rita Santos Passos-Bueno


Book ID
116433079
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
264 KB
Volume
51
Category
Article
ISSN
1769-7212

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