Matches in Nanopublications for { ?s ?p "[Autosomal recessive segregation of a truncating mutation of anti-Müllerian type II receptor in a family affected by the persistent Müllerian duct syndrome contrasts with its dominant negative activity in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP329641.RADWeFBAnmDNsQbpB3NETv4ica0_Xzt6ogFGbmGmwyvBQ130_assertion description "[Autosomal recessive segregation of a truncating mutation of anti-Müllerian type II receptor in a family affected by the persistent Müllerian duct syndrome contrasts with its dominant negative activity in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329641.RADWeFBAnmDNsQbpB3NETv4ica0_Xzt6ogFGbmGmwyvBQ130_provenance.
- NP421898.RAtKM68RBvySZiENb2igV-Rf35INROpqDX6bUQrOXD6cs130_assertion description "[Autosomal recessive segregation of a truncating mutation of anti-Müllerian type II receptor in a family affected by the persistent Müllerian duct syndrome contrasts with its dominant negative activity in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP421898.RAtKM68RBvySZiENb2igV-Rf35INROpqDX6bUQrOXD6cs130_provenance.
- NP1626.RAFwkvrx-CpAFN7LX67FioPdsQappLrx6tLwIAWaoAxQM130_assertion description "[Autosomal recessive segregation of a truncating mutation of anti-Müllerian type II receptor in a family affected by the persistent Müllerian duct syndrome contrasts with its dominant negative activity in vitro.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1626.RAFwkvrx-CpAFN7LX67FioPdsQappLrx6tLwIAWaoAxQM130_provenance.