Matches in Nanopublications for { ?s ?p "[Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP25906.RAO4H7dNnyYGCF6x-tWjUIRas3wPAQ8cpUEXp_gGuvR7M130_assertion description "[Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP25906.RAO4H7dNnyYGCF6x-tWjUIRas3wPAQ8cpUEXp_gGuvR7M130_provenance.
- NP25740.RAfdoKBuab_P8pdA-mZP0FRXX8MWg27lAc9Fd8nDuWMFM130_assertion description "[Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP25740.RAfdoKBuab_P8pdA-mZP0FRXX8MWg27lAc9Fd8nDuWMFM130_provenance.
- NP850267.RACD8EM5eJ4TxtQUJ4S0sSwUifhKVWLwapCIR0L3MZTUg130_assertion description "[Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP850267.RACD8EM5eJ4TxtQUJ4S0sSwUifhKVWLwapCIR0L3MZTUg130_provenance.
- NP387201.RAVBLklUBAryJd38j4UGFZB9Liq7fwaD_LRR0iJC4Ez9w130_assertion description "[Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387201.RAVBLklUBAryJd38j4UGFZB9Liq7fwaD_LRR0iJC4Ez9w130_provenance.
- assertion description "[Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP12764.RAuPbHV-gQ5i4iX2oNylgzs5TVyB92h-rTvcciXPfOQ98130_assertion description "[Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP12764.RAuPbHV-gQ5i4iX2oNylgzs5TVyB92h-rTvcciXPfOQ98130_provenance.
- NP387200.RAm0XMuE0mY7HgBORMVoiiOyLP-p-IKTiu6d1JwBYtI1w130_assertion description "[Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387200.RAm0XMuE0mY7HgBORMVoiiOyLP-p-IKTiu6d1JwBYtI1w130_provenance.