Matches in Nanopublications for { ?s ?p "[Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_assertion description "[Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP61102.RAi9NPpcm_X9Cju895Z-atNmXOHuWXI9juMx497yCwY-I130_provenance.
- NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_assertion description "[Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP95125.RAYdhOK0ZRrGkjoP-8L6lHAHvceEdBaud78AIHoX5Bokg130_provenance.
- assertion description "[Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_assertion description "[Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP128977.RATT1FpgLqjjdsxNbiu2dlJnL3EgRrPIatW_wqbvBiDSw130_provenance.
- assertion description "[Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP78763.RA1Kd04hdsWc5-pbieG0G6Ev5p8AKiRyVJQPCsR9-5-Ss130_assertion description "[Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP78763.RA1Kd04hdsWc5-pbieG0G6Ev5p8AKiRyVJQPCsR9-5-Ss130_provenance.
- NP128980.RAlz3kOSmFKxP-MaAXOatMXHJ45iw88kGEZNPLxU9GAqg130_assertion description "[Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP128980.RAlz3kOSmFKxP-MaAXOatMXHJ45iw88kGEZNPLxU9GAqg130_provenance.
- NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_assertion description "[Genetic analysis in patients with Kallmann syndrome: coexistence of mutations in prokineticin receptor 2 and KAL1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP689368.RA08PMKCfidT83C2aJuZpmVkUxsvuStkzn4ctJeMUTrqc130_provenance.