Matches in Nanopublications for { ?s ?p "[The wide variability of ocular phenotype regardless of the presence or absence of PAX6 mutations calls for a further appreciation of the complexity in the molecular diagnosis of aniridia and suggests that this ocular malformation may be better regarded as a group of heterogeneous disorders, rather than a single disease entity, associated with mutations in PAX6 and/or other genes located elsewhere in the human genome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP610283.RAY9yliyNaVrjJ4ej9i-doF-nqs-kLXcIa8MY-BCuu6f4130_assertion description "[The wide variability of ocular phenotype regardless of the presence or absence of PAX6 mutations calls for a further appreciation of the complexity in the molecular diagnosis of aniridia and suggests that this ocular malformation may be better regarded as a group of heterogeneous disorders, rather than a single disease entity, associated with mutations in PAX6 and/or other genes located elsewhere in the human genome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610283.RAY9yliyNaVrjJ4ej9i-doF-nqs-kLXcIa8MY-BCuu6f4130_provenance.
- assertion description "[The wide variability of ocular phenotype regardless of the presence or absence of PAX6 mutations calls for a further appreciation of the complexity in the molecular diagnosis of aniridia and suggests that this ocular malformation may be better regarded as a group of heterogeneous disorders, rather than a single disease entity, associated with mutations in PAX6 and/or other genes located elsewhere in the human genome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP962954.RAq3sj_kg9tCrobxC-73UqBqhgOtWUjyRXKEh-pnhL6zM130_assertion description "[The wide variability of ocular phenotype regardless of the presence or absence of PAX6 mutations calls for a further appreciation of the complexity in the molecular diagnosis of aniridia and suggests that this ocular malformation may be better regarded as a group of heterogeneous disorders, rather than a single disease entity, associated with mutations in PAX6 and/or other genes located elsewhere in the human genome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP962954.RAq3sj_kg9tCrobxC-73UqBqhgOtWUjyRXKEh-pnhL6zM130_provenance.