Angelman syndrome.
作者信息
Clayton-Smith J, Pembrey M E
机构信息
Department of Medical Genetics, St Mary's Hospital, Whitworth Park, Manchester.
出版信息
J Med Genet. 1992 Jun;29(6):412-5. doi: 10.1136/jmg.29.6.412.
Abstract
摘要
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本文引用的文献
1
The "happy puppet" syndrome.“快乐木偶”综合征。
Arch Dis Child. 1967 Jun;42(223):298-302. doi: 10.1136/adc.42.223.298.
2
The EEG in early diagnosis of the Angelman (happy puppet) syndrome.脑电图在天使综合征（快乐木偶综合征）早期诊断中的应用
Eur J Pediatr. 1988 Jun;147(5):508-13. doi: 10.1007/BF00441976.
3
The association of Angelman's syndrome with deletions within 15q11-13.安吉尔曼综合征与15q11 - 13区域内缺失的关联。
J Med Genet. 1989 Feb;26(2):73-7. doi: 10.1136/jmg.26.2.73.
4
Incidence of 15q deletions in the Angelman syndrome: a survey of twelve affected persons.天使综合征中15号染色体缺失的发生率：对12名患者的调查。
Am J Med Genet. 1989 Mar;32(3):339-45. doi: 10.1002/ajmg.1320320313.
5
On the parental origin of the deletion in Angelman syndrome.
Hum Genet. 1989 Sep;83(2):205-7. doi: 10.1007/BF00286723.
6
The 'happy puppet' syndrome of Angelman: review of the clinical features.安吉尔曼综合征的“快乐木偶”综合征：临床特征综述。
Arch Dis Child. 1989 Jan;64(1):83-6. doi: 10.1136/adc.64.1.83.
7
8
Angelman's syndrome.安吉尔曼综合征
J Med Genet. 1990 Apr;27(4):275-7. doi: 10.1136/jmg.27.4.275-a.
9
Angelman syndrome: three molecular classes identified with chromosome 15q11q13-specific DNA markers.安吉尔曼综合征：利用15q11q13染色体特异性DNA标记物鉴定出三种分子类型。
Am J Hum Genet. 1990 Jul;47(1):149-54.
10
DNA deletion and its parental origin in Angelman syndrome patients.天使综合征患者的DNA缺失及其亲本来源
Am J Med Genet. 1991 Oct 1;41(1):64-8. doi: 10.1002/ajmg.1320410117.
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