9qh+个体后代中9qh+的频率及染色体畸变风险。 - Suppr

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Frequency of 9qh+ and risk of chromosome aberrations in the progeny of individuals with 9qh+.

作者信息

Nielsen J, Friedrich U, Hreidarsson A B, Zeuthen E

出版信息

Humangenetik. 1974;21(3):211-6. doi: 10.1007/BF00279014.

DOI:10.1007/BF00279014

PMID:4136265

Abstract

摘要

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Frequency of 9qh+ and risk of chromosome aberrations in the progeny of individuals with 9qh+.9qh+个体后代中9qh+的频率及染色体畸变风险。

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本文引用的文献

CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). I. DATA ON A CONSECUTIVE SERIES OF PATIENTS REFERRED FOR GENETIC COUNSELLING AND DIAGNOSIS.唐氏综合征（先天愚型）的细胞遗传学。一、一系列因遗传咨询和诊断前来就诊患者的数据。

Cytogenetics. 1965;4:171-85. doi: 10.1159/000129853.

A familial variant of chromosome 9.9号染色体的家族性变异。

J Med Genet. 1971 Jun;8(2):202-8. doi: 10.1136/jmg.8.2.202.

Banding characteristics of paracentric marker constrictions in human chromosomes.人类染色体中臂内标记缢痕的带型特征。

Hereditas. 1972;70(2):309-10. doi: 10.1111/j.1601-5223.1972.tb01390.x.

Localization of heterochromatin in human chromosomes.人类染色体中异染色质的定位

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