Birth seasonality in Prader-Willi syndrome.
作者信息
Butler M G, Ledbetter D H, Mascarello J T
出版信息
Lancet. 1985 Oct 12;2(8459):828-9. doi: 10.1016/s0140-6736(85)90811-6.
Abstract
摘要
相似文献
1
Birth seasonality in Prader-Willi syndrome.普拉德-威利综合征的出生季节性
Lancet. 1985 Oct 12;2(8459):828-9. doi: 10.1016/s0140-6736(85)90811-6.
2
Season of birth and dyslexia.出生季节与诵读困难
J Am Acad Child Adolesc Psychiatry. 1993 Nov;32(6):1306-7. doi: 10.1016/S0890-8567(09)64907-8.
3
New onset epilepsy in Prader-Willi syndrome: semiology and literature review.普拉德-威利综合征中新发癫痫：症状学与文献复习。
Pediatr Neurol. 2010 Oct;43(4):297-9. doi: 10.1016/j.pediatrneurol.2010.05.015.
4
[The Prader-Willi syndrome and 15-15 translocation].[普拉德-威利综合征与15-15易位]
Ann Genet. 1977 Dec;20(4):297-300.
5
Deletion analysis of the imprinting center region in patients with Angelman syndrome and Prader-Willi syndrome by real-time quantitative PCR.通过实时定量PCR对天使综合征和普拉德-威利综合征患者印记中心区域进行缺失分析。
Genet Test. 2004 Winter;8(4):387-94. doi: 10.1089/gte.2004.8.387.
6
Diagnosis in Prader-Willi syndrome.普拉德-威利综合征的诊断
Arch Dis Child. 1994 Nov;71(5):441-2. doi: 10.1136/adc.71.5.441.
7
[Molecular diagnosis of Prader-Willi and Angelman syndromes: methylation, cytogenetics and FISH analysis].普拉德-威利综合征和安吉尔曼综合征的分子诊断：甲基化、细胞遗传学及荧光原位杂交分析
Rev Med Chil. 2001 Apr;129(4):367-74.
8
Prader-Willi syndrome with chromosome 15 interstitial deletion: report of one case.伴有15号染色体间质缺失的普拉德-威利综合征：1例报告。
Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi. 1991 Mar-Apr;32(2):105-11.
9
Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome.普拉德-威利综合征中15号染色体断点1和2之间4个基因的表达与行为结果
Pediatrics. 2006 Oct;118(4):e1276-83. doi: 10.1542/peds.2006-0424. Epub 2006 Sep 18.
10
Comparison of high resolution cytogenetics, fluorescence in situ hybridisation, and DNA studies to validate the diagnosis of Prader-Willi and Angelman's syndromes.高分辨率细胞遗传学、荧光原位杂交及DNA研究在普拉德-威利综合征和安吉尔曼综合征诊断验证中的比较
Arch Dis Child. 1995 May;72(5):397-402. doi: 10.1136/adc.72.5.397.
引用本文的文献
1
Birth seasonality studies in a large Prader-Willi syndrome cohort.大型普拉德-威利综合征队列中的出生季节性研究。
Am J Med Genet A. 2019 Aug;179(8):1531-1534. doi: 10.1002/ajmg.a.61263. Epub 2019 Jun 21.
2
Birth seasonality in Korean Prader-Willi syndrome with chromosome 15 microdeletion.韩国15号染色体微缺失型普拉德-威利综合征的出生季节性
Ann Pediatr Endocrinol Metab. 2015 Mar;20(1):40-5. doi: 10.6065/apem.2015.20.1.40. Epub 2015 Mar 31.
本文引用的文献
1
Chromosome 15 abnormalities and the Prader-Willi syndrome: a follow-up report of 40 cases.15号染色体异常与普拉德-威利综合征：40例随访报告
Am J Hum Genet. 1982 Mar;34(2):278-85.
2
Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 cases.普拉德-威利综合征与15号染色体。20例临床讨论
Hum Genet. 1983;64(4):356-62. doi: 10.1007/BF00292367.
3
Parental origin of de novo chromosome rearrangements.新发染色体重排的亲本来源。
Hum Genet. 1980;53(3):343-7. doi: 10.1007/BF00287054.
4
Chromosome abnormalities and season of birth.染色体异常与出生季节
Hum Genet. 1984;65(3):221-31. doi: 10.1007/BF00286507.
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.
7
8
Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome.39例普拉德-威利综合征患者的临床与细胞遗传学调查
Am J Med Genet. 1986 Mar;23(3):793-809. doi: 10.1002/ajmg.1320230307.
9
Clinical and cytogenetic studies of the Prader-Willi syndrome: evidence of phenotype-karyotype correlation.普拉德-威利综合征的临床与细胞遗传学研究：表型与核型相关性的证据
Hum Genet. 1985;69(1):22-7. doi: 10.1007/BF00295524.
10
Weather and human conception.天气与人类受孕
Psychol Rep. 1979 Jun;44(3 Pt 2):1241-2. doi: 10.2466/pr0.1979.44.3c.1241.
Zotero 插件