ArticleJournal of human genetics2015
Prenatal and postnatal findings in a 10.6 Mb interstitial deletion at 10p11.22-p12.31.
Article in Journal of human genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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Who cites it
1 citing paper in PubMed.
- Prenatal diagnosis of a pure 15q distal trisomy derived from a maternal pericentric inversion: A case report.Experimental and therapeutic medicine · 2021Article
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Authors and funding
9 authors.
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Abstract
Interstitial deletion of the proximal short arm of chromosome 10 represents a rare genetic alteration. Literature review revealed that only 10 postnatal diagnosed clinical cases with deletions overlapping 10p12p11 were published until present. We report the first prenatal diagnosis and postnatal findings in a male fetus with a 10.6 Mb interstitial deletion of the short arm of chromosome 10 (10p11.22-p12.31).
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Registered trials
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