Matches in Nanopublications for { ?s ?p "[We have defined the mutations causing congenital adrenal hyperplasia in three Swedish patients carrying a rare haplotype containing two mutated steroid 21-hydroxylase genes (CYP21) in addition to one pseudogene (CYP21P).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP1330387.RACBhv7J7X6wowXFVq3-xcv4aHHZlUh0haijYWw1_A2aA130_assertion description "[We have defined the mutations causing congenital adrenal hyperplasia in three Swedish patients carrying a rare haplotype containing two mutated steroid 21-hydroxylase genes (CYP21) in addition to one pseudogene (CYP21P).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1330387.RACBhv7J7X6wowXFVq3-xcv4aHHZlUh0haijYWw1_A2aA130_provenance.
- assertion description "[We have defined the mutations causing congenital adrenal hyperplasia in three Swedish patients carrying a rare haplotype containing two mutated steroid 21-hydroxylase genes (CYP21) in addition to one pseudogene (CYP21P).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[We have defined the mutations causing congenital adrenal hyperplasia in three Swedish patients carrying a rare haplotype containing two mutated steroid 21-hydroxylase genes (CYP21) in addition to one pseudogene (CYP21P).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1330388.RA_JDMmF8uieBs0tKR93eek7x1BQSr8hNFHNbN3n6HzGg130_assertion description "[We have defined the mutations causing congenital adrenal hyperplasia in three Swedish patients carrying a rare haplotype containing two mutated steroid 21-hydroxylase genes (CYP21) in addition to one pseudogene (CYP21P).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1330388.RA_JDMmF8uieBs0tKR93eek7x1BQSr8hNFHNbN3n6HzGg130_provenance.