| Predicate |
Object |
| contentType |
Journal Article|Review |
| endingPage |
10 |
| issn |
1096-7192 |
| issueIdentifier |
1 |
| pageRange |
1-10 |
| publicationName |
Molecular Genetics and Metabolism |
| startingPage |
1 |
| bibliographicCitation |
Osborne LR. Williams–Beuren Syndrome: Unraveling the Mysteries of a Microdeletion Disorder. Molecular Genetics and Metabolism. 1999 May;67(1):1–10. doi: 10.1006/mgme.1999.2844. |
| creator |
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_c45271b755af417ce3282e1a7044313e |
| date |
199905 |
| identifier |
https://pubmed.ncbi.nlm.nih.gov/10329018
https://doi.org/10.1006/mgme.1999.2844 |
| isPartOf |
https://portal.issn.org/resource/ISSN/1096-7192
http://rdf.ncbi.nlm.nih.gov/pubchem/journal/20853 |
| language |
English |
| source |
https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/ |
| title |
Williams–Beuren Syndrome: Unraveling the Mysteries of a Microdeletion Disorder |
| discusses |
http://id.nlm.nih.gov/mesh/M0007152 |
| hasPrimarySubjectTerm |
http://id.nlm.nih.gov/mesh/D017353
http://id.nlm.nih.gov/mesh/D018980Q000235 |
| hasSubjectTerm |
http://id.nlm.nih.gov/mesh/D004549Q000235
http://id.nlm.nih.gov/mesh/D002897
http://id.nlm.nih.gov/mesh/D006801
http://id.nlm.nih.gov/mesh/D010641
http://id.nlm.nih.gov/mesh/D005838
http://id.nlm.nih.gov/mesh/D002874 |