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K96243 gene equivalents contained within the 708a chromosome 1 deletion.

NIAID Data Ecosystem2026-03-07 收录

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https://figshare.com/articles/dataset/_K96243_gene_equivalents_contained_within_the_708a_chromosome_1_deletion_/552967 数据链接链接失效反馈

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1Annotation of BPSL1774 (mbaF) through BPSL1787 (mbaS) according to Alice et al. [30].

应用场景：

创建时间：

2013-02-21

消化道微生物组

细菌基因注释

Additional file 3. Flavonifractor sp. 54 gene annotations, including those that were defined as OTU41-characteristic genes. Definitions for columns are found in the first tab.

Figshare2021-02-18 更新40

Loss of 4q21.23-22.1 Is a Prognostic Marker for Disease Free and Overall Survival in Non-Small Cell Lung Cancer

非小细胞肺癌预后标志物

染色体缺失分析

This study was performed to assess the prognostic relevance of genomic aberrations at chromosome 4q in NSCLC patients. We have previously identified copy number changes at 4q12-q32 to be significantly

Figshare2016-01-15 更新30

Supplemental Material for Hirai et al. 2018

果蝇杂交不育遗传

染色体缺失分析

Table S7 The cross between Df(3R)/TM6C females and D. simulans Lhr males

Figshare2018-05-17 更新20

Coordinates of Xp11.22 deletions and Xp11.22 genes previously implicated or proposed to be involved in the development of intellectual disability/developmental delay/autism.

自闭症遗传学

染色体缺失分析

Coordinates of Xp11.22 deletions and Xp11.22 genes previously implicated or proposed to be involved in the development of intellectual disability/developmental delay/autism.

NIAID Data Ecosystem40

Genotyping data from one patient with unexplained mental retardation and a deletion in 15q13. Homo sapiens

神经遗传学

染色体缺失分析

Recurrent deletions on 15q13.3 have been identified as a predisposition to mental retardation, epilepsy and psychiatric disease. We report compound heterozygous deletions on 15q13.3 in one patients wi

NIAID Data Ecosystem20

K96243 gene equivalents contained within the 708a chromosome 1 deletion.

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