人类8号染色体。
Human chromosome 8.
作者信息
Wood S
机构信息
Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
出版信息
J Med Genet. 1988 Nov;25(11):721-31. doi: 10.1136/jmg.25.11.721.
Abstract
The role of human chromosome 8 in genetic disease together with the current status of the genetic linkage map for this chromosome is reviewed. Both hereditary genetic disease attributed to mutant alleles at gene loci on chromosome 8 and neoplastic disease owing to somatic mutation, particularly chromosomal translocations, are discussed.
摘要
本文综述了人类8号染色体在遗传疾病中的作用以及该染色体遗传连锁图谱的现状。文中讨论了归因于8号染色体基因座突变等位基因的遗传性遗传疾病，以及由于体细胞突变，特别是染色体易位引起的肿瘤性疾病。
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本文引用的文献
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Marble brain disease: recessive osteopetrosis, renal tubular acidosis and cerebral calcification in three Saudi Arabian families.大理石脑疾病：三个沙特阿拉伯家庭中的隐性骨硬化症、肾小管性酸中毒和脑钙化
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Tiny interstitial duplication of proximal 7q in association with a maternal paracentric inversion.近端7q微小间质重复伴母亲臂间倒位。
Hum Genet. 1982;62(2):113-6. doi: 10.1007/BF00282296.
5
Regulation of expression of liver-specific enzymes. II. Activation and chromosomal localization of soluble glutamate-pyruvate transaminase.肝脏特异性酶表达的调控。II. 可溶性谷氨酸丙酮酸转氨酶的激活及染色体定位
Ann Hum Genet. 1982 May;46(2):135-43. doi: 10.1111/j.1469-1809.1982.tb00704.x.
6
Assignment of the gene for cytosolic alanine aminotransferase (AAT1) to human chromosome 8.
Ann Hum Genet. 1982 May;46(2):125-33. doi: 10.1111/j.1469-1809.1982.tb00703.x.
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8
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