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[Are the mutation rates for the X-chromosomal forms of hemophilia in female gonads lower than in the gonads of males?].

作者信息

Vogel F

出版信息

Humangenetik. 1965;1(3):253-63. doi: 10.1007/BF00395656.

DOI:10.1007/BF00395656
PMID:5869749
Abstract
摘要

相似文献

1
[Are the mutation rates for the X-chromosomal forms of hemophilia in female gonads lower than in the gonads of males?].
Humangenetik. 1965;1(3):253-63. doi: 10.1007/BF00395656.
2
The effect of parental age on rates of mutation for hemophilia and evidence for differing mutation rates for hemophilia A and B.父母年龄对血友病突变率的影响以及血友病A和B不同突变率的证据。
Am J Hum Genet. 1968 May;20(3):175-96.
3
Segregation analysis of hemophilia A and B.甲型和乙型血友病的分离分析。
Am J Hum Genet. 1985 Jul;37(4):680-99.
4
Mutation rate in hemophilia A and B, and effect of parental age.
Bibl Haematol. 1966;26:91-3. doi: 10.1159/000384538.
5
The perpetuation of hemophilia by mutation.血友病因突变而持续存在。
Pediatrics. 1967 Feb;39(2):186-93.
6
From hemophilia B to hemophilia A via the fragile X locus: genes and recombination in the distal region of the human X chromosome long arm.从乙型血友病经脆性X位点到甲型血友病：人类X染色体长臂远端区域的基因与重组
Horiz Biochem Biophys. 1986;8:51-89.
7
[Gene mutation and gene diagnosis of hemophilia].[血友病的基因突变与基因诊断]
Nihon Seirigaku Zasshi. 1998;60(1):31-42.
8
Molecular basis of hemophilia.血友病的分子基础。
Hematol Pathol. 1990;4(1):1-26.
9
Genetics of hemorrhagic diathesis. Discussion.出血素质的遗传学。讨论
Thromb Diath Haemorrh Suppl. 1965;17:202-13.
10
Molecular basis of hemophilia.
Semin Hematol. 1990 Jul;27(3):270-85.

引用本文的文献

1
Characterization of the factor VIII defect in 147 patients with sporadic hemophilia A: family studies indicate a mutation type-dependent sex ratio of mutation frequencies.147例散发性甲型血友病患者凝血因子VIII缺陷的特征：家系研究表明突变频率的性别比取决于突变类型。
Am J Hum Genet. 1996 Apr;58(4):657-70.
2
Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.使用克隆的补体3基因探针进行强直性肌营养不良与19号染色体序列的连锁分析。
J Med Genet. 1983 Aug;20(4):259-63. doi: 10.1136/jmg.20.4.259.
3
Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention.

本文引用的文献

1
The mutation rate of the gene for haemophilia, and its segregation ratios in males and females.血友病基因的突变率及其在男性和女性中的分离比例。
Ann Eugen. 1947 Jun;13(4):262-71. doi: 10.1111/j.1469-1809.1946.tb02367.x.
2
Genetic Considerations in Familial Hemorrhagic Disease. I. The Sex-Linked Recessive Disorders, Hemophilia and PTC Deficiency.家族性出血性疾病的遗传学考量。I. 性连锁隐性疾病、血友病和血浆凝血活酶前体缺乏症。
Am J Hum Genet. 1963 Mar;15(1):53-61.
3
Sporadic cases of hemophilia and the question of a possible sex difference in mutation rates.
杜氏肌营养不良症：发病机制及基因预防
Hum Genet. 1984;66(1):17-40. doi: 10.1007/BF00275183.
4
[The effect of the age of the father at conception on the mutations to hemphilia A].
Humangenetik. 1966;3(1):1-16. doi: 10.1007/BF00273014.
5
[Genetic investigations in functional obstructive subvalvular aortic stenosis (irregular hypertrophic cardiomyopathy)].[功能性梗阻性主动脉瓣下狭窄（不规则肥厚型心肌病）的遗传学研究]
Humangenetik. 1968;6(1):13-28. doi: 10.1007/BF00287150.
6
Sex ratio of the mutation frequencies in haemophilia A: estimation and meta-analysis.甲型血友病突变频率的性别比：估计与荟萃分析。
Hum Genet. 1990 Dec;86(2):139-46. doi: 10.1007/BF00197695.
7
A probable sex difference in some mutation rates.某些突变率可能存在性别差异。
Am J Hum Genet. 1977 May;29(3):312-9.
血友病散发病例及突变率可能存在的性别差异问题。
Am J Hum Genet. 1962 Jun;14(2):159-69.
4
Carriers of hemophilia A: a laboratory study.甲型血友病携带者：一项实验室研究。
Acta Med Scand. 1959 Dec 5;165:357-70.
5
Formal genetics of muscular dystrophy.肌营养不良症的形式遗传学
Am J Hum Genet. 1959 Dec;11(4):360-79.
6
[Hereditary and sporadic genetic trees of hemophiliacs in Switzerland].[瑞士血友病患者的遗传和散发性遗传谱系]
Bull Schweiz Akad Med Wiss. 1954 Nov;10(5):303-421.
7
[SURVEYS ON THE DETERMINATION OF THE MUTATION RATE FOR HEMOPHILIA A AND B IN HAMBURG].
Z Mensch Vererb Konstitutionsl. 1963 Dec 17;37:251-68.
8
[THE HEREDITY OF HEMOPHILIA A].[甲型血友病的遗传]
Internist (Berl). 1963 Sep;4:397-400.
9
Haemophilia. A study of its laboratory, clinical, genetic and social aspects based on known haemophiliacs in Finland.
Scalpel (Brux). 1960;12(Suppl 46):1-144.
10
Estimates of the sex ratio of mutation rates in sex-linked conditions by the method of maximum likelihood.通过最大似然法对性连锁疾病中突变率的性别比进行估计。
Ann Hum Genet. 1958 May;22(3):244-9. doi: 10.1111/j.1469-1809.1958.tb01419.x.