Matches in DBpedia 2016-04 for { <https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1716407> ?p ?o }
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- PMC1716407 author "Waardenburg PJ".
- PMC1716407 date "September 1951".
- PMC1716407 first "P. J.".
- PMC1716407 isCitedBy ABCD_syndrome.
- PMC1716407 isCitedBy Petrus_Johannes_Waardenburg.
- PMC1716407 isCitedBy Waardenburg_syndrome.
- PMC1716407 issue "3".
- PMC1716407 journal American_Journal_of_Human_Genetics.
- PMC1716407 journal "Am. J. Hum. Genet.".
- PMC1716407 last "Waardenburg".
- PMC1716407 pages "195–253".
- PMC1716407 pmc "1716407".
- PMC1716407 pmid "14902764".
- PMC1716407 publisher American_Society_of_Human_Genetics.
- PMC1716407 title "A New Syndrome Combining Developmental Anomalies of the Eyelids, Eyebrows and Noseroot with Pigmentary Anomalies of the Iris and Head Hair and with Congenital Deafness; Dystopia canthi medialis et punctorum lacrimalium lateroversa, Hyperplasia supercilii medialis et radicis nasi, Heterochromia iridum totalis sive partialis, Albinismus circumscriptus et Surditas congenita".
- PMC1716407 title "A new syndrome combining developmental anomalies of the eyelids, eyebrows and noseroot with pigmentary anomalies of the iris and head hair and with congenital deafness".
- PMC1716407 title "A new syndrome combining developmental anomalies of the eyelids, eyebrows and noseroot with pigmentary anomalies of the iris and head hair and with congenital deafness; Dystopia canthi medialis et punctorum lacrimalium lateroversa, hyperplasia supercilii medialis et radicis nasi, heterochromia iridum totaliis sive partialis, albinismus circumscriptus et surditas congenita".
- PMC1716407 volume "3".