Matches in Nanopublications for { ?s ?p "[The PHF8 missense mutation c.836C>T is associated with mild MR, mild dysmorphic features, and either unilateral or bilateral cleft lip and cleft palate in two male siblings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP868353.RAYxO3QBJynYTQJPDAbX-aKSbWNx9fS8TN0Bgk0TPIef8130_assertion description "[The PHF8 missense mutation c.836C>T is associated with mild MR, mild dysmorphic features, and either unilateral or bilateral cleft lip and cleft palate in two male siblings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868353.RAYxO3QBJynYTQJPDAbX-aKSbWNx9fS8TN0Bgk0TPIef8130_provenance.
- assertion description "[The PHF8 missense mutation c.836C>T is associated with mild MR, mild dysmorphic features, and either unilateral or bilateral cleft lip and cleft palate in two male siblings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The PHF8 missense mutation c.836C>T is associated with mild MR, mild dysmorphic features, and either unilateral or bilateral cleft lip and cleft palate in two male siblings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP868352.RAvTdw9n6gz0nwkYGh_ozfReNgDKv-npoY2U_8I5mguYA130_assertion description "[The PHF8 missense mutation c.836C>T is associated with mild MR, mild dysmorphic features, and either unilateral or bilateral cleft lip and cleft palate in two male siblings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868352.RAvTdw9n6gz0nwkYGh_ozfReNgDKv-npoY2U_8I5mguYA130_provenance.
- NP770465.RANgj-Nu1CwpyJmpYFTeA_baIHT_WXgnUDyX9ZFvNga-U130_assertion description "[The PHF8 missense mutation c.836C>T is associated with mild MR, mild dysmorphic features, and either unilateral or bilateral cleft lip and cleft palate in two male siblings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP770465.RANgj-Nu1CwpyJmpYFTeA_baIHT_WXgnUDyX9ZFvNga-U130_provenance.
- NP770464.RAwYa7RScEv8FUzkWPS8SS7lyjJDCH9ogkRu-YxQLU6oA130_assertion description "[The PHF8 missense mutation c.836C>T is associated with mild MR, mild dysmorphic features, and either unilateral or bilateral cleft lip and cleft palate in two male siblings.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP770464.RAwYa7RScEv8FUzkWPS8SS7lyjJDCH9ogkRu-YxQLU6oA130_provenance.