Matches in Nanopublications for { ?s ?p "[New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_assertion description "[New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP4041.RArsxpRYkUgm4Xhh-pTgJGIAVRKeJFtd05682_PzTnIrc130_provenance.
- NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_assertion description "[New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164.RAWbgE9SVjGUkpG84Z1KZ7PZO40N6Z0cBNv7TfC5XyFfw130_provenance.
- assertion description "[New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1078.RASbnd03z13oZ_IONi2Lg-vGxDp8b-TwTZ6oxNN00Tpz0130_assertion description "[New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1078.RASbnd03z13oZ_IONi2Lg-vGxDp8b-TwTZ6oxNN00Tpz0130_provenance.
- NP297422.RA751VQV55Jz3byC34wAkGszhNrfR-Fva-9-ZY-l29UvY130_assertion description "[New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297422.RA751VQV55Jz3byC34wAkGszhNrfR-Fva-9-ZY-l29UvY130_provenance.
- NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_assertion description "[New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP297423.RA7d6XLAnJOBOCbrs0z2SLH7DViKKy8ON27sBVWjTuCsg130_provenance.