Matches in Nanopublications for { ?s ?p "[The sister also has a homozygous mutation in SLC45A2, which explains her severe oculocutaneous hypopigmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP587770.RA3fhUpiofc_LgYoVIghzwKvNC-RDOwyZQmxScZGYiBig130_assertion description "[The sister also has a homozygous mutation in SLC45A2, which explains her severe oculocutaneous hypopigmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587770.RA3fhUpiofc_LgYoVIghzwKvNC-RDOwyZQmxScZGYiBig130_provenance.
- NP248707.RAzhuvZrl8ucRdXJUKU7L88r1ou8kFk-MTocTUxmWaW1M130_assertion description "[The sister also has a homozygous mutation in SLC45A2, which explains her severe oculocutaneous hypopigmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP248707.RAzhuvZrl8ucRdXJUKU7L88r1ou8kFk-MTocTUxmWaW1M130_provenance.
- NP902402.RAZskYpZ-oMv0RJDSdqqkOynax7XPm5pT5jtuQvZ8lIog130_assertion description "[The sister also has a homozygous mutation in SLC45A2, which explains her severe oculocutaneous hypopigmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902402.RAZskYpZ-oMv0RJDSdqqkOynax7XPm5pT5jtuQvZ8lIog130_provenance.
- NP1030142.RA33z8c6AagBlo4E6uZm2v6JUZL_feHwI-PIEcsVCo_0s130_assertion description "[The sister also has a homozygous mutation in SLC45A2, which explains her severe oculocutaneous hypopigmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1030142.RA33z8c6AagBlo4E6uZm2v6JUZL_feHwI-PIEcsVCo_0s130_provenance.
- NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_assertion description "[The sister also has a homozygous mutation in SLC45A2, which explains her severe oculocutaneous hypopigmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902431.RANe25v2wIf4HfE9EQ5W3dn6z1UhHb4nU7mhV9a--QpXY130_provenance.
- NP1030141.RAgg0eH-TybXTj-Pu30B41UL3SBlIban0_Xuypgs2Rj9c130_assertion description "[The sister also has a homozygous mutation in SLC45A2, which explains her severe oculocutaneous hypopigmentation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1030141.RAgg0eH-TybXTj-Pu30B41UL3SBlIban0_Xuypgs2Rj9c130_provenance.