Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features is a research paper published in Human Mutation (2020). On theSindex it has a DataRank of 0. It has been cited 19 times.
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National Heart, Lung, and Blood Institute
Grant: HL006092
Intramural NIH HHS
Grant: Z99 HL999999
FWCI
1.44
Citation Percentile
0.8%
Citation Trend
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Sustainable Development Goals