File:Medi-100-e25777-g002 (1).jpg

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English: Prenatal diagnosis of 18p deletion syndrome in case 2. (A) The results of karyotype analysis: 46, XX, del (18)(p11.21). (B) The results of array-CGH:arr[GRCh37] 18p11.32p11.21 (146484-12532804)x1.
Date
Source https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8104293/
Author Qiujie Jin, Rong Qiang, Bo Cai, Xiaobin Wang, Na Cai, Shuai Zhen, and Wen Zhai

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{{subst:Custom license marker added by UW}} https://creativecommons.org/licenses/by/4.0/ Attribution 4.0 International (CC BY 4.0)

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