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Am J Hum Genet. 1994 Dec;55(6):1073-5.
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Paternal factors and schizophrenia risk: de novo mutations and imprinting.父系因素与精神分裂症风险：新发突变与印记
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3
Age and sex based genetic locus heterogeneity in type 1 diabetes.1型糖尿病中基于年龄和性别的基因座异质性。
J Med Genet. 2000 Mar;37(3):186-91. doi: 10.1136/jmg.37.3.186.
4
Rates of spontaneous mutation.自发突变率。
Genetics. 1998 Apr;148(4):1667-86. doi: 10.1093/genetics/148.4.1667.
5
Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma. Le Groupe d'Etude des Tumeurs a Calcitonine.2A型多发性内分泌腺瘤病和家族性甲状腺髓样癌中RET基因新发突变的患病率及亲本来源。降钙素瘤研究小组。
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6
Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23.11号染色体q23区域上家族性非嗜铬性副神经节瘤印记基因的精细定位
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本文引用的文献

1
The genetics of retinoblastoma, revisited.视网膜母细胞瘤的遗传学，再探讨。
Am J Hum Genet. 1994 Feb;54(2):264-73.
2
Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC.RET原癌基因的突变与2A型多发性内分泌腺瘤病和家族性甲状腺髓样癌相关。
Hum Mol Genet. 1993 Jul;2(7):851-6. doi: 10.1093/hmg/2.7.851.
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Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A.2A型多发性内分泌腺瘤病中RET原癌基因的种系突变。
Nature. 1993 Jun 3;363(6428):458-60. doi: 10.1038/363458a0.
4
Parent-of-origin effects in multiple endocrine neoplasia type 2B.2B型多发性内分泌腺瘤病中的亲本来源效应
Am J Hum Genet. 1994 Dec;55(6):1076-82.
5
Point mutation within the tyrosine kinase domain of the RET proto-oncogene in multiple endocrine neoplasia type 2B and related sporadic tumours.2B型多发性内分泌腺瘤及相关散发性肿瘤中RET原癌基因酪氨酸激酶结构域内的点突变。
Hum Mol Genet. 1994 Feb;3(2):237-41. doi: 10.1093/hmg/3.2.237.
6
Specific mutations of the RET proto-oncogene are related to disease phenotype in MEN 2A and FMTC.RET原癌基因的特定突变与2A型多发性内分泌腺瘤病（MEN 2A）和家族性甲状腺髓样癌（FMTC）的疾病表型相关。
Nat Genet. 1994 Jan;6(1):70-4. doi: 10.1038/ng0194-70.
7
A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma.一种与2B型多发性内分泌腺瘤病和散发性甲状腺髓样癌相关的RET原癌基因突变。
Nature. 1994 Jan 27;367(6461):375-6. doi: 10.1038/367375a0.
8
Single missense mutation in the tyrosine kinase catalytic domain of the RET protooncogene is associated with multiple endocrine neoplasia type 2B.RET原癌基因酪氨酸激酶催化结构域中的单个错义突变与2B型多发性内分泌肿瘤相关。
Proc Natl Acad Sci U S A. 1994 Feb 15;91(4):1579-83. doi: 10.1073/pnas.91.4.1579.
9
Imprinting: a gamete's point of view.印记：从配子的角度来看
Trends Genet. 1994 Jun;10(6):194-9. doi: 10.1016/0168-9525(94)90255-0.
10
Is there a relationship between sex of cystic fibrosis carriers and sex ratio of their offspring?
Hum Genet. 1980;54(1):79-82. doi: 10.1007/BF00279052.

Parental origin effects, genome imprinting, and sex-ratio distortion: double or nothing?

作者信息

Sapienza C

出版信息

Am J Hum Genet. 1994 Dec;55(6):1073-5.

PMID:7977364
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1918446/
Abstract
摘要