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染色体结构畸变对人类生殖健康的影响。II. 结果

The effect of structural aberrations of the chromosomes on reproductive fitness in man. II. Results.

作者信息

Jacobs P A, Frackiewicz A, Law P, Hilditch C J, Morton N E

出版信息

Clin Genet. 1975 Sep;8(3):169-78. doi: 10.1111/j.1399-0004.1975.tb01490.x.

Abstract

Reproductive fitness was measured in the following seven classes of pedigrees: (1) D/D Robertsonian translocations ascertained through a euploid proband; (2) D/G Robertsonian translocations ascertained through a euploid proband: (3) reciprocal translocations ascertained through a euploid proband; (4) inversions ascertained through a euploid proband; (5) all translocations and inversions ascertained through an aneuploid proband; (6) those ascertained through a proband with a ring, marker, or supernumerary chromosome; (7) those ascertained through a proband with an extreme variant chromosome. For each group reproductive fitness was calculated in two ways. One method was based on live births, fetal and infant deaths and generation time of those individuals carrying a chromosome abnormality or variant by comparison with their first degree relatives who were known to have a normal chromosome constitution. The second method was based on the proportion of sporadic cases obtained from segregation analysis. The results obtained using both methods are presented and discussed.

摘要

生殖适应性在以下七类谱系中进行了测量

(1)通过整倍体先证者确定的D/D罗伯逊易位;(2)通过整倍体先证者确定的D/G罗伯逊易位;(3)通过整倍体先证者确定的相互易位;(4)通过整倍体先证者确定的倒位;(5)通过非整倍体先证者确定的所有易位和倒位;(6)通过具有环状、标记或额外染色体的先证者确定的那些;(7)通过具有极端变异染色体的先证者确定的那些。对于每组,生殖适应性通过两种方式计算。一种方法基于携带染色体异常或变异的个体的活产、胎儿和婴儿死亡以及世代时间,并与已知具有正常染色体组成的一级亲属进行比较。第二种方法基于从分离分析中获得的散发病例比例。给出并讨论了使用这两种方法获得的结果。

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