Prenatal diagnosis and molecular cytogenetic analyses of a rare 15q21.3 and 16p11.2 microduplication family

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Publication Details

Journal
Molecular Cytogenetics
Published
2025-04-05
DOI
https://doi.org/10.1186/s13039-025-00711-w
Citations
1
Primary Topic
Genomic variations and chromosomal abnormalities
Type
article
Field-Weighted Citation Impact
1.82
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article

Prenatal diagnosis and molecular cytogenetic analyses of a rare 15q21.3 and 16p11.2 microduplication family

Xin Wen, G. R. Liao, Fei Zhang, Chengcheng Zhang
1 citations
Molecular Cytogenetics
Genomic variations and chromosomal abnormalities
1.82
article

Prenatal diagnosis and molecular cytogenetic analyses of a rare 15q21.3 and 16p11.2 microduplication family

Xin Wen, G. R. Liao, Fei Zhang, Chengcheng Zhang
article en
1 citations

Abstract

No abstract available for this paper.
Molecular CytogeneticsVol. 18(1)
Hubei Provincial Women and Children's Hospital (CN)
Zero hunger
Openalex Percentile: Top 17%
Genomic variations and chromosomal abnormalities
1.82
DOIOpen Access PDFOpenAlex
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Prenatal diagnosis and molecular cytogenetic analyses of a rare 15q21.3 and 16p11.2 microduplication family — Xin Wen, G. R. Liao, et al. · Molecular Cytogenetics (2025) | TGRS Research Map | TGRS