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对活产婴儿染色体的G带研究。

A G-band study of chromosomes in liveborn infants.

作者信息

Buckton K E, O'Riordan M L, Ratcliffe S, Slight J, Mitchell M, McBeath S, Keay A J, Barr D, Short M

出版信息

Ann Hum Genet. 1980 Jan;43(3):227-39. doi: 10.1111/j.1469-1809.1980.tb01556.x.

DOI:10.1111/j.1469-1809.1980.tb01556.x
PMID:7362200
Abstract

The results of a chromosome survey of 3993 liveborn infants, the majority of which have been studied using G-banding, are reported. The frequency of all types of chromosome abnormalities detected was similar to that found in previous newborn surveys, which were carried out on different socio-economic structure, but the incidence of aneuploid chromosome abnormalities was comparable in the two localities.

摘要

报告了对3993名活产婴儿进行染色体调查的结果,其中大多数婴儿已使用G显带技术进行研究。所检测到的各类染色体异常的频率与先前在不同社会经济结构中进行的新生儿调查中发现的频率相似,但两个地区非整倍体染色体异常的发生率相当。

相似文献

1
A G-band study of chromosomes in liveborn infants.对活产婴儿染色体的G带研究。
Ann Hum Genet. 1980 Jan;43(3):227-39. doi: 10.1111/j.1469-1809.1980.tb01556.x.
2
A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities.对14,069名新生儿的细胞遗传学调查。I. 染色体异常的发生率。
Clin Genet. 1975 Oct;8(4):223-43. doi: 10.1111/j.1399-0004.1975.tb01498.x.
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De novo t(5p;21q) in a patient previously diagnosed as monosomy 21.
Clin Genet. 1993 Feb;43(2):94-7. doi: 10.1111/j.1399-0004.1993.tb04457.x.
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Updating advances in cytogenetics. Applications of the new chromosome banding methods.细胞遗传学的最新进展。新染色体显带方法的应用。
Birth Defects Orig Artic Ser. 1974;10(8):7-18.
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[Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations].[荧光原位杂交(FISH)诊断非整倍体;在染色体畸变风险增加的妊娠中的价值]
Z Geburtshilfe Neonatol. 2000 Jan-Feb;204(1):1-7. doi: 10.1055/s-2000-10188.
6
Incidence of chromosome aberrations among 11148 newborn children.11148名新生儿的染色体畸变发生率。
Humangenetik. 1975 Oct 20;30(1):1-12. doi: 10.1007/BF00273626.
7
Spectral karyotyping and interphase FISH reveal abnormalities not detected by conventional G-banding. Implications for treatment stratification of childhood acute lymphoblastic leukaemia: detailed analysis of 70 cases.光谱核型分析和间期荧光原位杂交揭示了常规G显带未检测到的异常。对儿童急性淋巴细胞白血病治疗分层的意义:70例病例的详细分析。
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Chromosome studies in a neonatal population.新生儿群体的染色体研究。
Can Med Assoc J. 1972 Apr 8;106(7):776-9.
9
Antenatal diagnosis of chromosomal disorders.染色体疾病的产前诊断。
Clin Obstet Gynaecol. 1980 Apr;7(1):13-26.
10
[Clinical chromosome studies].[临床染色体研究]
Wien Klin Wochenschr. 1968 Oct 11;80(41):755-7 passim.

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Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population.大型生育人群中X和Y染色体非整倍体的发生率
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Directly transmitted unbalanced chromosome abnormalities and euchromatic variants.直接传递的不平衡染色体异常和常染色质变异
J Med Genet. 2005 Aug;42(8):609-29. doi: 10.1136/jmg.2004.026955.
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Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.使用普拉德-威利/安吉尔曼综合征区域特异性探针的inv dup(15)染色体分子细胞遗传学分析:临床意义
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Familial pericentric inversion inv(8)(p23q11).家族性臂间倒位inv(8)(p23q11)
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X-autosome translocations: cytogenetic characteristics and their consequences.X染色体与常染色体易位:细胞遗传学特征及其后果
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The frequency and mutation rate of balanced autosomal rearrangements in man estimated from prenatal genetic studies for advanced maternal age.根据针对高龄产妇的产前遗传学研究估算的人类常染色体平衡重排的频率和突变率。
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