Angelman syndrome (AS) is characterized by developmental delay, intellectual disability, movement or balance disorders, seizures, and limitations in speech and language development. Most cases of AS are caused by deletion in the 15q11-q13 region of the maternal chromosome. Prader-Willi syndrome (PWS) is a clinically distinct disorder resulting from paternal deletion of the 15q11-q13 region. Clinical features similar to AS are also shown in chromosome 15q11-q13 duplication syndrome. [provided by RefSeq, Jul 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| ANCRBA-20-REGO | 20 (40 μL) | 200 μL |
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| ANCRBA-20-REGR | 20 (40 μL) | 200 μL |
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| ANCRBA-20-ORGR | 20 (40 μL) | 200 μL |
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| ANCRBA-20-GOGR | 20 (40 μL) | 200 μL |
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| ANCRBA-20-GRRE | 20 (40 μL) | 200 μL |
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| ANCRBA-20-GROR | 20 (40 μL) | 200 μL |
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| ANCRBA-20-GRGO | 20 (40 μL) | 200 μL |
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| ANCRBA-20-AQOR | 20 (40 μL) | 200 μL |
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Angelman syndrome (AS) is characterized by developmental delay, intellectual disability, movement or balance disorders, seizures, and limitations in speech and language development. Most cases of AS are caused by deletion in the 15q11-q13 region of the maternal chromosome. Prader-Willi syndrome (PWS) is a clinically distinct disorder resulting from paternal deletion of the 15q11-q13 region. Clinical features similar to AS are also shown in chromosome 15q11-q13 duplication syndrome. [provided by RefSeq, Jul 2017]
Gene Symbol : ANCR
Gene Name : Angelman syndrome chromosome region
Locus : 15q11-q12
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