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- Q91790324 description "2019 թվականի հուլիսի 11-ին հրատարակված գիտական հոդված" @default.
- Q91790324 description "artículu científicu espublizáu en xunetu de 2019" @default.
- Q91790324 description "scientific article published on 11 July 2019" @default.
- Q91790324 description "wetenschappelijk artikel" @default.
- Q91790324 description "наукова стаття, опублікована 11 липня 2019" @default.
- Q91790324 name "Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome" @default.
- Q91790324 name "Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome" @default.
- Q91790324 type Item @default.
- Q91790324 label "Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome" @default.
- Q91790324 label "Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome" @default.
- Q91790324 prefLabel "Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome" @default.
- Q91790324 prefLabel "Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome" @default.
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- Q91790324 P2093 Q91790324-8029F25C-DCDC-4909-A2FD-6A4441DBA37A @default.
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- Q91790324 P304 Q91790324-CAFF2977-3CC6-4D31-9D33-933BE1D74E06 @default.
- Q91790324 P31 Q91790324-1D67219A-D3C9-4F7B-8262-AE241D345B3D @default.
- Q91790324 P356 Q91790324-8E744139-ADE6-4C2A-9ACE-E0FABB5E59F7 @default.
- Q91790324 P433 Q91790324-032DAAF2-BE76-4D37-ABB0-33FD3987588A @default.
- Q91790324 P478 Q91790324-971A91F6-F5DE-48BB-B3BB-F7754BDE0BA8 @default.
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- Q91790324 P50 Q91790324-F9E97B92-3494-48D7-B695-EA0F4B0F48F0 @default.
- Q91790324 P577 Q91790324-9974B8D4-40D4-494D-8CAC-C9C0C191CA1D @default.
- Q91790324 P698 Q91790324-17D37FDB-2DEA-4245-B423-9E007E5E8AFA @default.
- Q91790324 P356 AJMG.A.61281 @default.
- Q91790324 P698 31294511 @default.
- Q91790324 P1433 Q4744254 @default.
- Q91790324 P1476 "Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome" @default.
- Q91790324 P2093 "Amarilis Sanchez-Valle" @default.
- Q91790324 P2093 "Dan Doherty" @default.
- Q91790324 P2093 "Erin Torti" @default.
- Q91790324 P2093 "Gisele E Ishak" @default.
- Q91790324 P2093 "Hannah M Tully" @default.
- Q91790324 P2093 "Jane Juusola" @default.
- Q91790324 P2093 "Katrina M Dipple" @default.
- Q91790324 P2093 "Kirsty McWalter" @default.
- Q91790324 P2093 "Melissa Racobaldo" @default.
- Q91790324 P2093 "Taylor Sawyer" @default.
- Q91790324 P2093 "Whitney Neufeld-Kaiser" @default.
- Q91790324 P304 "1783-1790" @default.
- Q91790324 P31 Q13442814 @default.
- Q91790324 P356 "10.1002/AJMG.A.61281" @default.
- Q91790324 P433 "9" @default.
- Q91790324 P478 "179" @default.
- Q91790324 P50 Q87977147 @default.
- Q91790324 P50 Q88355920 @default.
- Q91790324 P50 Q91790320 @default.
- Q91790324 P577 "2019-07-11T00:00:00Z" @default.
- Q91790324 P698 "31294511" @default.