Matches in Wikidata for { <http://www.wikidata.org/entity/Q61647463> ?p ?o ?g. }
Showing items 1 to 55 of
55
with 100 items per page.
- Q61647463 description "article" @default.
- Q61647463 description "im August 2005 veröffentlichter wissenschaftlicher Artikel" @default.
- Q61647463 description "wetenschappelijk artikel" @default.
- Q61647463 description "наукова стаття, опублікована в серпні 2005" @default.
- Q61647463 name "An Uncommon Phenotype with Familial Central Hypogonadism Caused by a NovelPROP1Gene Mutant Truncated in the Transactivation Domain" @default.
- Q61647463 name "An Uncommon Phenotype with Familial Central Hypogonadism Caused by a NovelPROP1Gene Mutant Truncated in the Transactivation Domain" @default.
- Q61647463 type Item @default.
- Q61647463 label "An Uncommon Phenotype with Familial Central Hypogonadism Caused by a NovelPROP1Gene Mutant Truncated in the Transactivation Domain" @default.
- Q61647463 label "An Uncommon Phenotype with Familial Central Hypogonadism Caused by a NovelPROP1Gene Mutant Truncated in the Transactivation Domain" @default.
- Q61647463 prefLabel "An Uncommon Phenotype with Familial Central Hypogonadism Caused by a NovelPROP1Gene Mutant Truncated in the Transactivation Domain" @default.
- Q61647463 prefLabel "An Uncommon Phenotype with Familial Central Hypogonadism Caused by a NovelPROP1Gene Mutant Truncated in the Transactivation Domain" @default.
- Q61647463 P1433 Q61647463-6AE05135-C885-4EAF-B979-372D2E3868EB @default.
- Q61647463 P1476 Q61647463-A22923AD-C892-4219-8D01-2855D0400FAF @default.
- Q61647463 P2093 Q61647463-2FBE7ECE-4BE0-4FB7-B375-2C8F9310D027 @default.
- Q61647463 P2093 Q61647463-889088C8-6A74-4135-A57E-B08FE4AB4327 @default.
- Q61647463 P2093 Q61647463-8BAD6351-0787-43DA-A0B7-4573554C5E57 @default.
- Q61647463 P2093 Q61647463-C1C00E87-CE05-45AD-9AC7-9F75CC4F2041 @default.
- Q61647463 P2093 Q61647463-DAE0D45B-9249-4FF7-88F4-A8EE1959154D @default.
- Q61647463 P2093 Q61647463-F570012F-F910-42D8-A32F-B7E182C40911 @default.
- Q61647463 P304 Q61647463-6E9CC9C6-07E6-4D4A-8DFA-C29870A41509 @default.
- Q61647463 P31 Q61647463-28C50913-F8DE-403D-A5AD-38B79D68F8D9 @default.
- Q61647463 P356 Q61647463-E04D5F2C-A4A1-4BEF-8FE9-8810DA94525F @default.
- Q61647463 P407 Q61647463-4AE950FD-315E-49E6-AFDA-90789F9943AD @default.
- Q61647463 P433 Q61647463-833AADD2-2EA9-4C4F-B3FB-FF83B31EBFC7 @default.
- Q61647463 P478 Q61647463-F4B10B30-02AA-403F-B888-0128D94E24B3 @default.
- Q61647463 P50 Q61647463-1EA5FF53-EF8A-4548-A7C6-7ECE8D1A6277 @default.
- Q61647463 P50 Q61647463-253682BB-3831-4DC9-8CF3-1C2AAC32649B @default.
- Q61647463 P50 Q61647463-AAC82BA9-6366-466E-8D07-47A25B42473A @default.
- Q61647463 P577 Q61647463-FB9715C0-93FF-43F2-BD3D-193F78EB1C30 @default.
- Q61647463 P698 Q61647463-948B6AD5-BFC7-403B-818D-6D938C28054D @default.
- Q61647463 P921 Q61647463-98634E5F-0234-44A1-9B1E-6DCB8891B8AB @default.
- Q61647463 P921 Q61647463-A0F1C8CE-6E71-4253-86B9-2312979724B2 @default.
- Q61647463 P356 JC.2005-0119 @default.
- Q61647463 P698 15941866 @default.
- Q61647463 P1433 Q3186902 @default.
- Q61647463 P1476 "An uncommon phenotype with familial central hypogonadism caused by a novel PROP1 gene mutant truncated in the transactivation domain" @default.
- Q61647463 P2093 "Alain Enjalbert" @default.
- Q61647463 P2093 "Gilbert Simonin" @default.
- Q61647463 P2093 "Marie-Pierre Guillet" @default.
- Q61647463 P2093 "Paul Valensi" @default.
- Q61647463 P2093 "Rachel Reynaud" @default.
- Q61647463 P2093 "Sophie Vallette-Kasic" @default.
- Q61647463 P304 "4880-4887" @default.
- Q61647463 P31 Q13442814 @default.
- Q61647463 P356 "10.1210/JC.2005-0119" @default.
- Q61647463 P407 Q1860 @default.
- Q61647463 P433 "8" @default.
- Q61647463 P478 "90" @default.
- Q61647463 P50 Q40173582 @default.
- Q61647463 P50 Q40207746 @default.
- Q61647463 P50 Q42842237 @default.
- Q61647463 P577 "2005-06-07T00:00:00Z" @default.
- Q61647463 P698 "15941866" @default.
- Q61647463 P921 Q104053 @default.
- Q61647463 P921 Q938107 @default.