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- Q77205238 description "article scientifique publié en 2001" @default.
- Q77205238 description "artículu científicu espublizáu n'ochobre de 2001" @default.
- Q77205238 description "im Oktober 2001 veröffentlichter wissenschaftlicher Artikel" @default.
- Q77205238 description "scientific article published on 01 October 2001" @default.
- Q77205238 description "wetenschappelijk artikel" @default.
- Q77205238 description "наукова стаття, опублікована в жовтні 2001" @default.
- Q77205238 name "A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene" @default.
- Q77205238 name "A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene" @default.
- Q77205238 type Item @default.
- Q77205238 label "A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene" @default.
- Q77205238 label "A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene" @default.
- Q77205238 prefLabel "A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene" @default.
- Q77205238 prefLabel "A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene" @default.
- Q77205238 P1433 Q77205238-5563613D-9A49-4531-9D23-9CCBEA5D904B @default.
- Q77205238 P1476 Q77205238-AA7284E6-3413-445B-8A99-9AF2B09D32D6 @default.
- Q77205238 P2093 Q77205238-0B001BE4-1C46-43BF-8D00-A99D87326C9A @default.
- Q77205238 P2093 Q77205238-4137237C-C8BF-4FA9-AAA4-374D34BD22E1 @default.
- Q77205238 P2093 Q77205238-5F1BCA28-D75C-4C32-BCFA-BF71454E1409 @default.
- Q77205238 P2093 Q77205238-BF2EB7F5-1A62-4817-A571-A31D399C7915 @default.
- Q77205238 P2093 Q77205238-D68F5248-4605-4153-9E82-F66AF2A2923C @default.
- Q77205238 P2093 Q77205238-F5544315-FAFD-46A1-A771-8062FEF43075 @default.
- Q77205238 P304 Q77205238-794DF88C-F813-47F1-9F62-B88842447A60 @default.
- Q77205238 P31 Q77205238-F8710181-1E11-4C13-882F-A01DF176E766 @default.
- Q77205238 P356 Q77205238-42FF8A7A-C5C0-4AC3-AFDE-2FD67C3B49B0 @default.
- Q77205238 P433 Q77205238-9FDEA48A-5F71-43A6-AACC-001ABE748F7E @default.
- Q77205238 P478 Q77205238-F8BB8235-EDF9-421A-9CE6-26B13809D578 @default.
- Q77205238 P577 Q77205238-1DD17BA8-1277-4EAB-A483-182CC3A0E09C @default.
- Q77205238 P698 Q77205238-174A4C5D-1C61-494E-A4C5-B2E69D6E1B11 @default.
- Q77205238 P921 Q77205238-1E594146-942A-41D3-9915-04AD19922154 @default.
- Q77205238 P921 Q77205238-5E9D365B-2CEA-41C7-AE8A-496F1E477B60 @default.
- Q77205238 P356 105072501753211064 @default.
- Q77205238 P698 11716047 @default.
- Q77205238 P1433 Q15709940 @default.
- Q77205238 P1476 "A familial case of congenital hypothyroidism caused by a homozygous mutation of the thyrotropin receptor gene" @default.
- Q77205238 P2093 "Bretones P" @default.
- Q77205238 P2093 "David M" @default.
- Q77205238 P2093 "Duprez L" @default.
- Q77205238 P2093 "Parma J" @default.
- Q77205238 P2093 "Rodien P" @default.
- Q77205238 P2093 "Vassart G" @default.
- Q77205238 P304 "977-980" @default.
- Q77205238 P31 Q13442814 @default.
- Q77205238 P356 "10.1089/105072501753211064" @default.
- Q77205238 P433 "10" @default.
- Q77205238 P478 "11" @default.
- Q77205238 P577 "2001-10-01T00:00:00Z" @default.
- Q77205238 P698 "11716047" @default.
- Q77205238 P921 Q114049690 @default.
- Q77205238 P921 Q531012 @default.