Parental origin of chromosome 15 deletion in Prader-Willi syndrome.
作者信息
Butler M G, Palmer C G
出版信息
Lancet. 1983 Jun 4;1(8336):1285-6. doi: 10.1016/s0140-6736(83)92745-9.
Abstract
摘要
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本文引用的文献
1
Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.15号染色体缺失是普拉德-威利综合征的病因。
N Engl J Med. 1981 Feb 5;304(6):325-9. doi: 10.1056/NEJM198102053040604.
2
Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome.普拉德-威利综合征的掌指纹型分析
Clin Genet. 1982 Dec;22(6):315-20. doi: 10.1111/j.1399-0004.1982.tb01846.x.
3
Human Gene Mapping 6. Oslo conference (1981). Sixth International Workshop on Human Gene Mapping.人类基因定位6. 奥斯陆会议（1981年）。第六届人类基因定位国际研讨会。
Birth Defects Orig Artic Ser. 1982;18(2):1-341.
4
On the structure and polymorphism of the human chromosome no. 15.关于人类15号染色体的结构与多态性
Hum Genet. 1980;56(1):115-8. doi: 10.1007/BF00281580.
5
Syndrome of hypotonia-hypomentia-hypogonadism-obesity (HHHO) or Prader-Willi syndrome.肌张力减退-智力减退-性腺功能减退-肥胖综合征（HHHO）或普拉德-威利综合征。
Am J Dis Child. 1968 May;115(5):588-98. doi: 10.1001/archpedi.1968.02100010590009.
6
Prader-Willi syndrome. A resumé of 32 cases including an instance of affected first cousins, one of whom is of normal stature and intelligence.普拉德-威利综合征。32例病例总结，包括一对患病的堂兄妹，其中一人身材和智力正常。
J Pediatr. 1972 Aug;81(2):286-93. doi: 10.1016/s0022-3476(72)80297-x.
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