与HLA连锁的基因Bf、C2、C4S、C4F、21-羟化酶缺乏症和乙二醛酶I的基因频率及遗传连锁不平衡 - Suppr

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超能文献

Gene frequencies and genetic linkage disequilibrium for the HLA-linked genes Bf, C2, C4S, C4F, 21-hydroxylase deficiency, and glyoxalase I.

作者信息

O'Neill G J, Pollack M S, Yang S Y, Levine L S, New M I, Dupont B

出版信息

Transplant Proc. 1979 Dec;11(4):1713-5.

PMID:316936

Abstract

摘要

相似文献

Gene frequencies and genetic linkage disequilibrium for the HLA-linked genes Bf, C2, C4S, C4F, 21-hydroxylase deficiency, and glyoxalase I.与HLA连锁的基因Bf、C2、C4S、C4F、21-羟化酶缺乏症和乙二醛酶I的基因频率及遗传连锁不平衡

Transplant Proc. 1979 Dec;11(4):1713-5.

Data on linkage relations between GLO and 21-hydroxylase.

Hum Genet. 1980;54(3):419-20. doi: 10.1007/BF00291592.

Polymorphism of glyoxalase I in Vienna.维也纳乙二醛酶I的多态性

Hum Hered. 1979;29(4):204-7. doi: 10.1159/000153044.

Heterozygotes and cryptic patients in families of patients with congenital adrenal hyperplasia (21-hydroxylase deficiency). HLA and glyoxalase I typing and hormonal studies.先天性肾上腺皮质增生症（21-羟化酶缺乏症）患者家系中的杂合子和隐匿性患者。HLA和乙二醛酶I分型及激素研究。

Horm Res. 1982;16(3):151-9. doi: 10.1159/000179496.

Genetics and biochemical variability of variants of 21 hydroxylase deficiency.21-羟化酶缺乏症变异体的遗传学和生化变异性

J Med Genet. 1985 Oct;22(5):354-60. doi: 10.1136/jmg.22.5.354.

[Genetic of the 21 hydroxylase deficiency].[21-羟化酶缺乏症的遗传学]

Ann Endocrinol (Paris). 1982;43(1):3-14.

Genetics of congenital adrenal hyperplasia.

Prog Clin Biol Res. 1985;200:233-41.

Linkage relationship of C2 deficiency, HLA and glyoxalase I loci.补体C2缺陷、人类白细胞抗原（HLA）和乙二醛酶I基因座的连锁关系。

Vox Sang. 1979;37(6):321-8. doi: 10.1111/j.1423-0410.1979.tb02311.x.

The HLA associations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a Yugoslav population.

Ann N Y Acad Sci. 1985;458:36-40. doi: 10.1111/j.1749-6632.1985.tb14587.x.

No linkage disequilibrium HLA-GLO found in 1,004 normal, unrelated Danes.在1004名正常、无亲缘关系的丹麦人中未发现HLA - GLO连锁不平衡。

Hum Hered. 1981;31(1):15-8. doi: 10.1159/000153170.

引用本文的文献

History of Adrenal Research: From Ancient Anatomy to Contemporary Molecular Biology.肾上腺研究史：从古代解剖学到当代分子生物学。

Endocr Rev. 2023 Jan 12;44(1):70-116. doi: 10.1210/endrev/bnac019.

High frequency of nonclassical steroid 21-hydroxylase deficiency.非经典型类固醇21-羟化酶缺乏症的高发病率。

Am J Hum Genet. 1985 Jul;37(4):650-67.

HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiency.意大利经典型21-羟化酶缺乏症患者的HLA基因型及HLA连锁遗传标记

Hum Genet. 1981;58(3):331-7. doi: 10.1007/BF00294933.

HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency.HLA连锁以及B14、DR1、BfS单倍型与迟发性和隐匿性21-羟化酶缺乏症相关基因的关联。

Am J Hum Genet. 1981 Jul;33(4):540-50.

Immunofixation for C2 typing: C2 allotypes in Spaniards in relation to HLA, Bf and C4.用于C2分型的免疫固定法：西班牙人中C2同种异型与HLA、Bf和C4的关系。

Hum Genet. 1985;71(1):58-61. doi: 10.1007/BF00295670.

Order of class III genes relative to HLA genes determined by the haplotype method.通过单倍型方法确定的Ⅲ类基因相对于HLA基因的顺序。

Immunogenetics. 1986;24(2):79-83. doi: 10.1007/BF00373113.

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