Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation (Q24538533)
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Current Data About Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation
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(P1476) "Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no phenotype-genotype correlation" (language: en)
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(P2093) Birgitt Schüle
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Angelica Oviedo
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Kathreen Johnston
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Shashidhar Pai
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Uta Francke
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