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3 |
| issn |
1096-8628
0148-7299 |
| issueIdentifier |
1 |
| pageRange |
1-3 |
| publicationName |
American Journal of Medical Genetics |
| startingPage |
1 |
| bibliographicCitation |
Cohen MM. Unclassifiable craniosynostosis phenotypes, FGFR2 Trp290 mutations, acanthosis nigricans, and unpaired cysteine mutations. Am J Med Genet. 2002 Nov 15;113(1):1–3. doi: 10.1002/ajmg.10748. PMID: 12400057. |
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http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0df9242f316c6a2c95b2a415e114dcaa |
| date |
2002-09-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| identifier |
https://doi.org/10.1002/ajmg.10748
https://pubmed.ncbi.nlm.nih.gov/12400057 |
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http://rdf.ncbi.nlm.nih.gov/pubchem/journal/434
https://portal.issn.org/resource/ISSN/1096-8628 |
| language |
English |
| source |
https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/ |
| title |
Unclassifiable craniosynostosis phenotypes,FGFR2Trp290 mutations, acanthosis nigricans, and unpaired cysteine mutations |
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