Christmas disease in one of a pair of monozygotic twin girls, possibly the effect of lyonization.
作者信息
Révész T, Schuler D, Goldschmidt B, Elödi S
出版信息
J Med Genet. 1972 Dec;9(4):396-400. doi: 10.1136/jmg.9.4.396.
Abstract
摘要
相似文献
1
Christmas disease in one of a pair of monozygotic twin girls, possibly the effect of lyonization.一对同卵双胞胎女孩中的一个患有克里斯马斯病，可能是莱昂化的结果。
J Med Genet. 1972 Dec;9(4):396-400. doi: 10.1136/jmg.9.4.396.
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[Lyonization as a possible cause of hemophilia B in a female child].[莱昂化作用作为一名女童患B型血友病的可能病因]
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Hemophilia B (Christmas disease) in a female.女性患血友病B（克里斯马斯病）。
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Discordant identical twins. Christmas disease.不一致的同卵双胞胎。克里斯马斯病。
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Christmas disase in a female.一名女性患克里斯马斯病。
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Female twins with severe Christmas disease (hemophilia B).患有严重圣诞病（血友病B）的女性双胞胎。
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Coeliac disease in monozygotic twin girls. Synchronous presentation.单卵双胞胎女孩中的乳糜泻。同步发病。
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Christmas disease in a girl.一名女孩患克里斯马斯病。
Am J Dis Child. 1969 May;117(5):585-8. doi: 10.1001/archpedi.1969.02100030587016.
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X inactivation patterns in female monozygotic twins and their families.女性同卵双胞胎及其家族中的X染色体失活模式。
J Med Genet. 1994 Oct;31(10):754-7. doi: 10.1136/jmg.31.10.754.
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Duchenne muscular dystrophy in one of monozygotic twin girls.单卵双胞胎女孩中的一个患有杜氏肌营养不良症。
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Twinning and mitotic crossing-over: some possibilities and their implications.孪生与有丝分裂交换：一些可能性及其影响。
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Different patterns of X inactivation in MZ twins discordant for red-green color-vision deficiency.在同卵双胞胎中，红绿色觉缺陷不一致的个体存在不同的X染色体失活模式。
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The phenotypic range of hemophilia A carriers.甲型血友病携带者的表型范围。
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Progressive myoclonus epilepsy. A variant with probable X-linked inheritance.
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本文引用的文献
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Morphology and enumeration of human blood platelets.人体血小板的形态学与计数
J Appl Physiol. 1950 Dec;3(6):365-77. doi: 10.1152/jappl.1950.3.6.365.
2
Haemophilia A in a "girl" with male sex-chromatin pattern.
Lancet. 1959 Sep 5;2(7097):264-6. doi: 10.1016/s0140-6736(59)92058-6.
3
Erythrocyte glucose-6-phosphate dehydrogenase deficiency: evidence of differences between Negroes and Caucasians with respect to this genetically determined trait.红细胞葡萄糖-6-磷酸脱氢酶缺乏症：关于这一由基因决定的性状，黑人和白种人之间存在差异的证据。
J Clin Invest. 1959 Dec;38(12):2253-62. doi: 10.1172/JCI104006.
4
Monozygotic and dizygotic twin diagnosis.单卵双胎和双卵双胎诊断。
Ann Hum Genet. 1955 Jun;19(4):273-89. doi: 10.1111/j.1469-1809.1955.tb01354.x.
5
Christmas factor: dosage compensation and the production of blood coagulation factor IX.克里斯马斯因子：剂量补偿与凝血因子IX的产生
Science. 1963 Jan 25;139(3552):348-9. doi: 10.1126/science.139.3552.348.
6
Detection of carriers for factor IX (PTC) deficiency.检测因子IX（PTC）缺乏症的携带者。
Blood. 1962 Aug;20:150-5.
7
Chromosome preparations of leukocytes cultured from human peripheral blood.从人外周血培养的白细胞的染色体标本制备。
Exp Cell Res. 1960 Sep;20:613-6. doi: 10.1016/0014-4827(60)90138-5.
8
Anti-hemophilic globulin levels in carriers of hemophilia A.甲型血友病携带者的抗血友病球蛋白水平。
J Clin Invest. 1960 Nov;39(11):1619-25. doi: 10.1172/JCI104184.
9
The partial thromboplastin time with kaolin. A simple screening test for first stage plasma clotting factor deficiencies.高岭土部分凝血活酶时间。用于筛查第一阶段血浆凝血因子缺乏症的简单检测。
Am J Clin Pathol. 1961 Sep;36:212-9. doi: 10.1093/ajcp/36.3.212.
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