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Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features
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Journal Title: | Human Mutation |
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Authors and Corporations: | , , , , , , , , , , , , , , |
In: | Human Mutation, 41, 2020, 7, p. 1238-1249 |
Type of Resource: | E-Article |
Language: | English |
published: |
Hindawi Limited
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