There are several phenotypes associated with variation in pericentric region of chromosome 16: see the 16p12.2-p11.2 deletion syndrome (MIM 613604); see MIM 611913 for a deletion or duplication at 16p11.2 associated with autism (AUTS14); and see MIM 613444 for a 220-kb deletion at 16p11.2 associated with isolated severe early-onset obesity and obesity with developmental delay.[supplied by OMIM, Nov 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| FRA16A-20-RE | 20 (40 μL) | 200 μL |  |
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| FRA16A-20-OR | 20 (40 μL) | 200 μL |  |
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| FRA16A-20-GO | 20 (40 μL) | 200 μL |  |
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| FRA16A-20-GR | 20 (40 μL) | 200 μL |  |
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| FRA16A-20-AQ | 20 (40 μL) | 200 μL |  |
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There are several phenotypes associated with variation in pericentric region of chromosome 16: see the 16p12.2-p11.2 deletion syndrome (MIM 613604); see MIM 611913 for a deletion or duplication at 16p11.2 associated with autism (AUTS14); and see MIM 613444 for a 220-kb deletion at 16p11.2 associated with isolated severe early-onset obesity and obesity with developmental delay.[supplied by OMIM, Nov 2010]
Gene Symbol : FRA16A
Gene Name : Fragile site, folic acid type, rare, fra(16)(p13.11)
Chromosome : CHR 16: 0-0
Locus : 16p13.11
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