NTCC® NA23832 LCL DNA-BioVector NTCC典型培养物保藏中心Coriell NA23832
- 价 格:¥59850
- 货 号:NTCC®-Coriell NA23832
- 产 地:北京
- BioVector NTCC典型培养物保藏中心
- 联系人:Dr.Xu, Biovector NTCC Inc.
电话:400-800-2947 工作QQ:1843439339 (微信同号)
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地址:北京
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Name:NTCC® NA23832 LCL DNACategory分类:DNACat#货号:NTCC®-Coriell NA23832Size/Quantity数量: 1 VialBiosafety Level生物安全级别:1Shipping Info运输方式: RTStorage储存方式: 4CSpecies物种来源: Age年龄: 1 YRGender性别: FemaleDescription描述: PRADER-WILLI SYNDROME; PWSRemarks: Affected; mother had gestational diabetes which was well controlled; subject required intubation from birth until day of life 4; supplemental feeding by NG tube; mild micrognathia; anteverted tip of the nose; high-arched palate; short and broad neck; low anterior and posterior hairline; generalized mild hypotonia; short stature; bilateral astigmatism; strabismus; early onset morbid obesity, primarily abdominal fat distribution; mildly hypoplastic labia minora; tapered fingers; short 4th and 5th metacarpals; mild scoliosis; obstructive sleep apnea; staring episodes, but no seizures; microsatellite testing revealed maternal uniparental disomy of chromosome 15; normal head ultrasound; normal echo; borderline prolonged QT segment on EKG; head MRI showed delayed myelination pattern; swallow study revealed silent aspiration in supine position only; development assessment using Bayley Scale of Infant Development at approximately 12 months revealed cognitive score:65 (low), language (74) borderline, motor (61) low, social-emotional (60) low, general adaptive (53), low; treatments include occupational therapy, physical therapy and growth hormone.
Alternate IDs其他编号: Cell Type细胞类型:
LCLSource组织来源: LCLGene: SNRPN Disease疾病类型: Mutations突变: DEL MATERNAL EXON ALPHAKaryotypes核型: Cytogenetics: Mutation description突变描述: Origin: Transformants: Alias别名: Images图片:References参考文献:Supplier供应商:BioVector质粒载体菌株细胞蛋白抗体基因保藏中心
NTCC典型培养物保藏中心
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