Prader-Willi syndrome: Methylation study or fluorescence in situ hybridization first.

Hamzi, Khalil; Itto, Afaf Ben; Nassereddine, Sanaa; Nadifi, Sellama

Hamzi, Khalil; Itto, Afaf Ben; Nassereddine, Sanaa; Nadifi, Sellama.

Indian J Hum Genet ; 2010 Sept; 16(3): 172-174

Article in En | IMSEAR | ID: sea-138921

Subject(s)

Child, Preschool; Female; Humans; Intellectual Disability/etiology; In Situ Hybridization, Fluorescence/methods; Methylation; Obesity/etiology; Parents; Prader-Willi Syndrome/diagnosis; Prader-Willi Syndrome/epidemiology; Prader-Willi Syndrome/etiology; Prader-Willi Syndrome/genetics; Respiration/abnormalities

Key words

Fluorescence in situ hybridization; methylation; obesity; Prader–Willi syndrome

Fulltext

Add to My VHL

XML

Search on Google

Full text: 1 Index: IMSEAR Main subject: Parents / Prader-Willi Syndrome / Respiration / Female / Humans / Child, Preschool / In Situ Hybridization, Fluorescence / Intellectual Disability / Methylation / Obesity Language: En Journal: Indian J Hum Genet Year: 2010 Type: Article

Fulltext

Add to My VHL

XML

Search on Google