Matches in Wikidata for { <http://www.wikidata.org/entity/Q85028767> ?p ?o ?g. }
Showing items 1 to 46 of
46
with 100 items per page.
- Q85028767 description "artículu científicu espublizáu en setiembre de 2011" @default.
- Q85028767 description "im September 2011 veröffentlichter wissenschaftlicher Artikel" @default.
- Q85028767 description "scientific article published on 30 September 2011" @default.
- Q85028767 description "wetenschappelijk artikel" @default.
- Q85028767 description "наукова стаття, опублікована у вересні 2011" @default.
- Q85028767 name "Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters" @default.
- Q85028767 name "Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters" @default.
- Q85028767 type Item @default.
- Q85028767 label "Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters" @default.
- Q85028767 label "Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters" @default.
- Q85028767 prefLabel "Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters" @default.
- Q85028767 prefLabel "Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters" @default.
- Q85028767 P1433 Q85028767-65206FD3-82B3-4FF3-923B-F307C41D3E3E @default.
- Q85028767 P1476 Q85028767-67A581AE-3E1F-48F4-A666-A55B6C8D2E93 @default.
- Q85028767 P2093 Q85028767-9C43EF58-E6E6-47D4-9DE4-7F12A3DFA7A3 @default.
- Q85028767 P2093 Q85028767-BC1C8F61-29BE-4096-9EDA-9A19D9E9978B @default.
- Q85028767 P2093 Q85028767-C72ABAA7-BB1F-4562-BA62-1F13C2AD480D @default.
- Q85028767 P2093 Q85028767-E126EE6B-1C66-40D2-9B3A-F5CBAE4861C3 @default.
- Q85028767 P2093 Q85028767-FDC01CDA-2271-443B-B585-803BD1E696F5 @default.
- Q85028767 P304 Q85028767-88777D7E-E8C4-4B80-8BC0-CE9748183172 @default.
- Q85028767 P31 Q85028767-086947FF-13FC-48BE-99C3-B824F0B47B00 @default.
- Q85028767 P356 Q85028767-62CECB67-2254-4EA8-995D-17543B7CC89C @default.
- Q85028767 P433 Q85028767-5F0EE951-0A76-4888-A3C2-968AF2F83EDA @default.
- Q85028767 P478 Q85028767-8E9215CE-AD69-47CE-9F96-873708BFDC61 @default.
- Q85028767 P50 Q85028767-026B293E-F2FC-4115-B36D-189AA3FC28D1 @default.
- Q85028767 P577 Q85028767-F2BEE182-E6CA-4B63-94D6-7250070C2902 @default.
- Q85028767 P698 Q85028767-E4A936CA-4815-4CCD-B830-DCC3E27477D2 @default.
- Q85028767 P921 Q85028767-52F93FD8-0C6A-4EBB-971A-C8902B56B001 @default.
- Q85028767 P356 AJMG.A.34255 @default.
- Q85028767 P698 21964664 @default.
- Q85028767 P1433 Q4744254 @default.
- Q85028767 P1476 "Compound heterozygous deletion of NRXN1 causing severe developmental delay with early onset epilepsy in two sisters" @default.
- Q85028767 P2093 "Edward Blair" @default.
- Q85028767 P2093 "Joanna McParland" @default.
- Q85028767 P2093 "Lyndsey Connell" @default.
- Q85028767 P2093 "Michael G Pike" @default.
- Q85028767 P2093 "Victoria Harrison" @default.
- Q85028767 P304 "2826-2831" @default.
- Q85028767 P31 Q13442814 @default.
- Q85028767 P356 "10.1002/AJMG.A.34255" @default.
- Q85028767 P433 "11" @default.
- Q85028767 P478 "155A" @default.
- Q85028767 P50 Q60642716 @default.
- Q85028767 P577 "2011-09-30T00:00:00Z" @default.
- Q85028767 P698 "21964664" @default.
- Q85028767 P921 Q124059385 @default.