The human POP2 gene: identification, sequencing, and mapping to the critical region of the 5q- syndrome.

Fidler C; Wainscoat JS; Boultwood J

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The human POP2 gene: identification, sequencing, and mapping to the critical region of the 5q- syndrome.

机译：人类POP2基因：鉴定，测序和定位到5q-综合征的关键区域。

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来源
《Genomics》 |1999年第1期|共3页
作者
Fidler C; Wainscoat JS; Boultwood J;
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原文格式 PDF
正文语种 eng
中图分类遗传学;
关键词
Chromosomes; Human; Pair 5; Myelodysplastic Syndromes; Transcription Factors; 染色体; 人; 5对; 骨髓增生异常综合征; 转录因子;

机译：Chromosomes;Human;Pair 5;Myelodysplastic Syndromes;Transcription Factors;染色体;人;5对;骨髓增生异常综合征;转录因子;

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专利

1. The human POP2 gene: identification, sequencing, and mapping to the critical region of the 5q- syndrome. [J] . Fidler C, Wainscoat JS, Boultwood J Genomics . 1999,第1期

机译：人类POP2基因：鉴定，测序和定位到5q-综合征的关键区域。
2. Physical mapping of the human ATX1 homologue (HAH1) to the critical region of the 5q- syndrome within 5q32, and immediately adjacent to the SPARC gene. [J] . Boultwood J, Strickson AJ, Jabs EW, Human Genetics . 2000,第1期

机译：将人ATX1同源物（HAH1）物理映射到5q32内5q-综合征的关键区域，并紧邻SPARC基因。
3. Molecular cytogenetic delineation of the critical deleted region in the 5q- syndrome. [J] . Jaju RJ, Boultwood J, Oliver FJ, Genes, Chromosomes and Cancer . 1998,第3期

机译：5q-综合征关键缺失区域的分子细胞遗传学描述。
4. Homozygosity Mapping using Whole-Exome Sequencing: A Valuable Approach for Pathogenic Variant Identification in Genetic Diseases [C] . Jorge Oliveira, Rute Pereira, Rosario Santos, International Conference on Bioinformatics Models, Methods and Algorithms . 2017

机译：纯合子映射使用全exome测序：一种有价值的遗传疾病致病变异鉴定的方法
5. Fine-structure mapping and sequencing of the origin of replication and the microheterogeneity regions of bovine herpesvirus 1 DNA. [D] . Westerman, Karen Ann. 1992

机译：牛疱疹病毒1 DNA的复制起点和微异质性区域的精细结构定位和测序。
6. Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families [O] . Hanan E. Shamseldin, Maha Tulbah, Wesam Kurdi, 2015

机译：通过自噬映射和近亲家庭外显子组测序鉴定人类胚胎致死基因
7. Array comparative genomic hybridization in patients with congenital diaphragmatic hernia: mapping of four CDH-critical regions and sequencing of candidate genes at 15q26.1–15q26.2 [O] . Anne M Slavotinek, Ali Moshrefi, Randy Davis, 2006

机译：先天性膈疝患者的阵列比较基因组杂交：15〜26.1-15〜15〜15〜5〜15〜15季度候选基因测定的映射。

The human POP2 gene: identification, sequencing, and mapping to the critical region of the 5q- syndrome.

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