| Property | Value |
|---|
| Working Groups |  RG Wollnik |
| Subproject | None |
| Open Access |  Yes |
| Publication Type | Journal Article |
| Peer Reviewed | Yes |
| PMID |  34629465 |
| DOI |  10.1038/s41431-021-00967-x |
| Publication Year | 2021 |
| Title | Familial cleft tongue caused by a unique translation initiation codon variant in TP63  |
| Journal | European Journal of Human Genetics |
| ISSN | 1018-4813 |
| eISSN | 1476-5438 |
| URL | http://dx.doi.org/10.1038/s41431-021-00967-x |
| Journal Abbreviation | Eur J Hum Genet |
| Authors | Schmidt J, Schreiber G, Altmüller J, Thiele H, Nürnberg P, Li Y, Kaulfuß S, Funke R, Wilken B, Yigit G, Wollnik B |
| First Author | Schmidt J |
| Last Author | Wollnik B |
| Scholia |  Wikidata-based representation at Scholia |
External Resources
nature.c...-x.pdfhttps://www.nature.com/articles/s41431-021-00967-x.pdf
Article fulltext
gro-2/94604http://resolver.sub.uni-goettingen.de/purl?gro-2/94604
GRO.publications identifier
9606https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?id=9606
NCBI taxonomy (human, Homo sapiens)
0000-0002-5942-2924https://orcid.org/0000-0002-5942-2924
ORCID identifier (Julia Schmidt)
0000-0003-2777-0198https://orcid.org/0000-0003-2777-0198
ORCID identifier (Gökhan Yigit)
0000-0003-2589-0364https://orcid.org/0000-0003-2589-0364
ORCID identifier (Bernd Wollnik)
05xy1nn52https://ror.org/05xy1nn52
ROR identifier (05xy1nn52, Multiscale Bioimaging)
021ft0n22https://ror.org/021ft0n22
ROR identifier (021ft0n22, University Medical Center Göttingen)
SCR_018393https://scicrunch.org/resolver/SCR_018393
SciCrunch identifier (RRID:SCR_018393, Combined Annotation Dependent Depletion)
SCR_002344https://scicrunch.org/resolver/SCR_002344
SciCrunch identifier (RRID:SCR_002344, Ensembl)
SCR_014964https://scicrunch.org/resolver/SCR_014964
SciCrunch identifier (RRID:SCR_014964, Genome Aggregation Database)
SCR_016386https://scicrunch.org/resolver/SCR_016386
SciCrunch identifier (RRID:SCR_016386, Illumina HiSeq 3000/HiSeq 4000 System)
SCR_010777https://scicrunch.org/resolver/SCR_010777
SciCrunch identifier (RRID:SCR_010777, MutationTaster)
SCR_006472https://scicrunch.org/resolver/SCR_006472
SciCrunch identifier (RRID:SCR_006472, NCBI)
SCR_013189https://scicrunch.org/resolver/SCR_013189
SciCrunch identifier (RRID:SCR_013189, PolyPhen)
SCR_012813https://scicrunch.org/resolver/SCR_012813
SciCrunch identifier (RRID:SCR_012813, SIFT)
SCR_005780https://scicrunch.org/resolver/SCR_005780
SciCrunch identifier (RRID:SCR_005780, UCSC Genome Browser)
mbexc.de...-tp63/https://mbexc.de/familial-cleft-tongue-caused-by-a-unique-translation-initiation-codon-variant-in-tp63/
Website entry (mbexc.de)
Q112812680https://www.wikidata.org/wiki/Q112812680
Wikidata ID
