文献
J-GLOBAL ID:200902245050364458
整理番号:09A0023431
歯牙崩出の家族性で非症候群性の原発性不全におけるPTHR1機能損失突然変異
PTHR1 Loss-of-Function Mutations in Familial, Nonsyndromic Primary Failure of Tooth Eruption
著者 (11件):
DECKER Eva
(Inst. of Human Genetics, Univ. of Regensburg, Regensburg 93053, DEU)
,
DECKER Eva
(Inst. of Human Genetics, Univ. of Heidelberg, Heidelberg 69120, DEU)
,
STELLZIG-EISENHAUER Angelika
(Dep. of Orthodontics, Univ. of Wuerzburg, Wuerzburg 97070, DEU)
,
FIEBIG Britta S.
(Inst. of Human Genetics, Univ. of Regensburg, Regensburg 93053, DEU)
,
RAU Christiane
(Dep. of Orthodontics, Univ. of Wuerzburg, Wuerzburg 97070, DEU)
,
KRESS Wolfram
(Inst. of Human Genetics, Univ. of Wuerzburg, Wuerzburg 97074, DEU)
,
SAAR Kathrin
(Max Delbrueck Center for Molecular Medicine, Berlin 13092, DEU)
,
RUESCHENDORF Franz
(Max Delbrueck Center for Molecular Medicine, Berlin 13092, DEU)
,
HUBNER Norbert
(Max Delbrueck Center for Molecular Medicine, Berlin 13092, DEU)
,
GRIMM Tiemo
(Inst. of Human Genetics, Univ. of Wuerzburg, Wuerzburg 97074, DEU)
,
WEBER Bernhard H.F.
(Inst. of Human Genetics, Univ. of Regensburg, Regensburg 93053, DEU)
資料名:
American Journal of Human Genetics
(American Journal of Human Genetics)
巻:
83
号:
6
ページ:
781-786
発行年:
2008年12月12日
JST資料番号:
B0360B
ISSN:
0002-9297
資料種別:
逐次刊行物 (A)
発行国:
オランダ (NLD)
言語:
英語 (EN)