Mutations in STAG2 cause an X-linked cohesinopathy associated with undergrowth, developmental delay, and dysmorphia: Expanding the phenotype in males. (Q64981381)
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scientific article published on 16 November 2018
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English | Mutations in STAG2 cause an X-linked cohesinopathy associated with undergrowth, developmental delay, and dysmorphia: Expanding the phenotype in males. |
scientific article published on 16 November 2018 |
Statements
Mutations in STAG2 cause an X-linked cohesinopathy associated with undergrowth, developmental delay, and dysmorphia: Expanding the phenotype in males. (English)
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Sureni V Mullegama
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Rebecca H Signer
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UCLA Clinical Genomics Center
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Eric Vilain
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16 November 2018
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