| Predicate |
Object |
| contentType |
Journal Article |
| endingPage |
6 |
| issn |
0971-6866 |
| issueIdentifier |
3 |
| pageRange |
245-6 |
| publicationName |
Indian Journal of Human Genetics |
| startingPage |
245 |
| bibliographicCitation |
Nagaveni NB, Umashankara KV. Hay-Wells syndrome of ectodermal dysplasia: A rare autosomal dominant disorder. Indian J Hum Genet. 2011 Sep;17(3):245–6. PMID: 22346004; PMCID: PMC3277001. |
| creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_bc9dfbe2d9c0414ee604ef67f30d493b
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_2d930d3dd30066e5121c62f9612b5689 |
| date |
201109 |
| identifier |
https://doi.org/10.4103/0971-6866.92084
https://pubmed.ncbi.nlm.nih.gov/22346004
https://pubmed.ncbi.nlm.nih.gov/PMC3277001 |
| isPartOf |
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/36604
https://portal.issn.org/resource/ISSN/0971-6866 |
| language |
English |
| source |
https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/ |
| title |
Hay-Wells syndrome of ectodermal dysplasia: A rare autosomal dominant disorder |
| discussesAsDerivedByTextMining |
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID7541
http://rdf.ncbi.nlm.nih.gov/pubchem/disease/DZID647 |