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常染色体易位男性的不育症:14;22罗伯逊易位的减数分裂研究

Infertility in human males with autosomal translocations: meiotic study of a 14;22 Robertsonian translocation.

作者信息

Guichaoua M R, Quack B, Speed R M, Noel B, Chandley A C, Luciani J M

机构信息

Département d'Embryologie et de Cytogénétique, Faculté de Médecine, Marseille, France.

出版信息

Hum Genet. 1990 Dec;86(2):162-6. doi: 10.1007/BF00197698.

Abstract

Pachytene analysis was undertaken in a male patient heterozygous for a 14q22q Robertsonian translocation. The relatively low rate of XY autosome association led us to examine the relationships existing between the chromosomes involved in the translocation, the rate of XY-autosome association and the degree of spermatogenic failure. Cytogenetic investigations in infertile men and the results of the meiotic studies suggest a direct correlation between the frequency of XY-autosome association at pachytene and the degree of spermatogenic failure. Whether associations arise as a consequence or cause of germ cell failure is still not certain.

摘要

对一名携带14q22q罗伯逊易位的男性杂合子患者进行了粗线期分析。XY常染色体联会率相对较低,这促使我们研究参与易位的染色体之间存在的关系、XY-常染色体联会率以及生精失败的程度。对不育男性的细胞遗传学研究和减数分裂研究结果表明,粗线期XY-常染色体联会频率与生精失败程度之间存在直接相关性。联会是生殖细胞失败的结果还是原因仍不确定。

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