Chromosome Aberrations; Comparative Genomic Hybridization; Embryo, Mammalian; Female; Genetic Screening; Humans; In Situ Hybridization, Fluorescence; Microarray Analysis; Polymorphism, Single Nucleotide; Pregnancy

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Chromosome Aberrations; Comparative Genomic Hybridization; Embryo, Mammalian; Female; Genetic Screening; Humans; In Situ Hybridization, Fluorescence; Microarray Analysis; Polymorphism, Single Nucleotide; Pregnancy

机译：染色体畸变;比较基因组杂交;胚胎，哺乳动物;女;基因筛选;人类;原位杂交，荧光;芯片分析;多态性，单核苷酸;怀孕

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《AIDS care.》 |2009年第6期|共9页
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1. Chromosome Aberrations; Comparative Genomic Hybridization; Embryo, Mammalian; Female; Genetic Screening; Humans; In Situ Hybridization, Fluorescence; Microarray Analysis; Polymorphism, Single Nucleotide; Pregnancy [J] . AIDS care. . 2009,第6期

机译：染色体畸变;比较基因组杂交;胚胎，哺乳动物;女;基因筛选;人类;原位杂交，荧光;芯片分析;多态性，单核苷酸;怀孕
2. Novel 1.3 Mb germline duplication in chromosome 8q21.11 by microarray comparative genomic hybridization?plus single nucleotide polymorphism analysis in an adult patient with pancytopenia and urinary bladder complications [J] . Cynthia Reyes Barron, Andrew G. Evans, Hiroshi Miyamoto, Clinical Case Reports . 2018,第10期

机译：成年患者全血细胞减少和膀胱并发症的微阵列比较基因组杂交与单核苷酸多态性分析在染色体8q21.11中的新型1.3 Mb生殖系重复
3. Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization. [J] . Chen CP, Kuo YT, Lin SP, Taiwanese journal of obstetrics and gynecology . 2010,第3期

机译：镶嵌环形染色体18，环形染色体18复制/缺失和二体化18：围产期发现和通过荧光原位杂交和阵列比较基因组杂交的分子细胞遗传学表征。
4. Microarray-based approach for high-throughput genotyping of single nucleotide polymorphisms with Layer-by-Layer dual-color fluorescence hybridization [C] . . 2005

机译：基于微阵列的单核苷酸多态性高通量基因分型方法与逐层双色荧光杂交
5. Detection of genomic deletions by single-nucleotide polymorphism array comparative genomic hybridization. [D] . Stanczak, Krzysztof M. 2007

机译：通过单核苷酸多态性阵列比较基因组杂交检测基因组缺失。
6. Novel 1.3 Mb germline duplication in chromosome 8q21.11 by microarray comparative genomic hybridization plus single nucleotide polymorphism analysis in an adult patient with pancytopenia and urinary bladder complications [O] . Cynthia Reyes Barron, Andrew G. Evans, Hiroshi Miyamoto, 2018

机译：通过微阵列比较基因组杂交加上单核苷酸多态性分析对成年全血细胞减少症和膀胱并发症的成年患者进行新型1.3 Mb生殖细胞8q21.11染色体复制
7. Significance of Chromosomal Aberrations in CLL. Concerning Jarošová M, et al.: Contribution of comparative genomic hybridization and fluorescence in situ hybridization to the detection of chromosomal abnormalities in B-cell chronic lymphocytic leukemia. Onkologie 2001;24:60–65. [O] . L. Bergmann 2001

机译：Cl1中染色体畸变的意义。关于Jarošovám，等，：对比基因组杂交和荧光原位杂交的贡献，以检测B细胞慢性淋巴细胞白血病染色体异常。 Onkologie 2001; 24：60-65。

Chromosome Aberrations; Comparative Genomic Hybridization; Embryo, Mammalian; Female; Genetic Screening; Humans; In Situ Hybridization, Fluorescence; Microarray Analysis; Polymorphism, Single Nucleotide; Pregnancy

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