CASE REPORT
Published on 19 Jul 2022
Case Report: Prenatal Identification of a De Novo Mosaic Neocentric Marker Resulting in 13q31.1→qter Tetrasomy in a Mildly Affected Girl
doi 10.3389/fgene.2022.906077
- 1,774 views
- 1 citation
- Frontiers in Genetics
- Human and Medical Genomics
- Research Topics
- The Role of Large Genome Structural Variants in Human Health and Disease
The Role of Large Genome Structural Variants in Human Health and Disease
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Articles
ORIGINAL RESEARCH
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ORIGINAL RESEARCH
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doi 10.3389/fgene.2021.789625
- 1,661 views
- 1 citation
ORIGINAL RESEARCH
Published on 17 Sep 2021
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doi 10.3389/fgene.2021.732419
- 3,391 views
- 17 citations
ORIGINAL RESEARCH
Published on 20 Oct 2020
Analysis of Chromosomal Copy Number in First-Trimester Pregnancy Loss Using Next-Generation Sequencing
doi 10.3389/fgene.2020.545856
- 4,105 views
- 19 citations
ORIGINAL RESEARCH
Published on 22 Sep 2020
Deletion of FUNDC2 and CMC4 on Chromosome Xq28 Is Sufficient to Cause Hypergonadotropic Hypogonadism in Men
doi 10.3389/fgene.2020.557341
- 3,898 views
- 10 citations
Published in
Frontiers in Genetics
- Human and Medical Genomics
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- 23kTopic views
- 18kArticle views
- 5,165Article downloads