Matches in Nanopublications for { ?s ?p "[Autosomal dominant inactivating sprouty-related EVH1 domain-containing protein 1 (SPRED1) mutations have recently been described in individuals presenting mainly with caf� au lait macules (CALMs), axillary freckling, and macrocephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP860690.RAUXBSEvRjWeMQJ8WPrCWyjqPJspoKoa8q7kMDkZMwKCk130_assertion description "[Autosomal dominant inactivating sprouty-related EVH1 domain-containing protein 1 (SPRED1) mutations have recently been described in individuals presenting mainly with caf� au lait macules (CALMs), axillary freckling, and macrocephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP860690.RAUXBSEvRjWeMQJ8WPrCWyjqPJspoKoa8q7kMDkZMwKCk130_provenance.
- NP977311.RABQfFrnAkfQCUaq3b2iiEN4Lpo6gVEMXbfDgi5-kBvug130_assertion description "[Autosomal dominant inactivating sprouty-related EVH1 domain-containing protein 1 (SPRED1) mutations have recently been described in individuals presenting mainly with caf� au lait macules (CALMs), axillary freckling, and macrocephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP977311.RABQfFrnAkfQCUaq3b2iiEN4Lpo6gVEMXbfDgi5-kBvug130_provenance.
- NP776359.RAhm4SsNYjuINORC6dmF7maUupZSa3UUJJzsTsekNXsRY130_assertion description "[Autosomal dominant inactivating sprouty-related EVH1 domain-containing protein 1 (SPRED1) mutations have recently been described in individuals presenting mainly with caf� au lait macules (CALMs), axillary freckling, and macrocephaly.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP776359.RAhm4SsNYjuINORC6dmF7maUupZSa3UUJJzsTsekNXsRY130_provenance.