Analysis of 13q RFLP in multiple endocrine neoplasia type II kindreds.
作者信息
Deschamps M, Butler M G, Phillips J A
出版信息
Cancer Genet Cytogenet. 1987 Nov;29(1):183-5. doi: 10.1016/0165-4608(87)90049-5.
Abstract
摘要
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本文引用的文献
1
Age-related probability of development of hereditary medullary thyroid carcinoma.遗传性甲状腺髓样癌发生的年龄相关概率。
J Pediatr. 1982 Dec;101(6):941-6. doi: 10.1016/s0022-3476(82)80014-0.
2
Chromosome 20 deletion in human multiple endocrine neoplasia types 2A and 2B: a double-blind study.人类2A型和2B型多发性内分泌腺瘤中20号染色体缺失：一项双盲研究。
Proc Natl Acad Sci U S A. 1984 Apr;81(8):2525-8. doi: 10.1073/pnas.81.8.2525.
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Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.从人类13号染色体中分离并对揭示多态性位点的DNA片段进行区域定位。
Am J Hum Genet. 1984 Jan;36(1):10-24.
4
The genes for growth hormone and chorionic somatomammotropin are on the long arm of human chromosome 17 in region q21 to qter.生长激素基因和绒毛膜生长催乳素基因位于人类第17号染色体长臂的q21至qter区域。
Hum Genet. 1981;57(2):138-41. doi: 10.1007/BF00282009.
5
Genetic origin of mutations predisposing to retinoblastoma.视网膜母细胞瘤易感性突变的遗传起源。
Science. 1985 Apr 26;228(4698):501-3. doi: 10.1126/science.3983638.
6
Recessive mutant genes predisposing to human cancer.易引发人类癌症的隐性突变基因。
Mutat Res. 1986 Jul;168(1):3-14. doi: 10.1016/0165-1110(86)90019-9.
7
High resolution chromosome and DNA analysis in multiple endocrine neoplasia type II syndrome.II型多发性内分泌腺瘤综合征的高分辨率染色体和DNA分析
Cancer Genet Cytogenet. 1987 Jan;24(1):129-35. doi: 10.1016/0165-4608(87)90089-6.
8
Linkage analysis of a DNA marker localized to 20p12 and multiple endocrine neoplasia type 2A.定位于20p12的DNA标记与2A型多发性内分泌腺瘤的连锁分析。
Am J Hum Genet. 1985 Sep;37(5):890-7.
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Detection of specific sequences among DNA fragments separated by gel electrophoresis.在通过凝胶电泳分离的DNA片段中检测特定序列。
J Mol Biol. 1975 Nov 5;98(3):503-17. doi: 10.1016/s0022-2836(75)80083-0.
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