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Whole‐exome sequencing revealed a nonsense mutation in STKLD1 causing non‐syndromic pre‐axial polydactyly type A affecting only upper limb
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Journal Title: | Clinical Genetics |
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Authors and Corporations: | , , , , , , , , , , |
In: | Clinical Genetics, 96, 2019, 2, p. 134-139 |
Type of Resource: | E-Article |
Language: | English |
published: |
Wiley
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Subjects: |