Next Generation Sequencing and Sanger Sequencing of the COL11A2 gene

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Documentation:
Ref: LV1448 Categories: , , , , , , , Diseases: Deafness, Autosomal Recessive 53,Fibrochondrogenesis 2,Nonsyndromic Hearing Loss and Deafness, Autosomal Dominant type 13,Otospondylomegaepiphyseal dysplasia,Stickler syndrome, type III,Weissenbacher-Zweymuller syndromeGenes: COL11A2Delivery term: 42 days
sistemas genómicos
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