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GENOTYPE-PHENOTYPE CORRELATIONS OF TWO RARER GAUCHER DISEASE MUTATIONS
被引:0
作者
:
King, L. Sniderman
论文数:
0
引用数:
0
h-index:
0
机构:
Seattle Childrens Hosp, Div Med Genet, Seattle, WA USA
Seattle Childrens Hosp, Div Med Genet, Seattle, WA USA
King, L. Sniderman
[
1
]
Hale, S.
论文数:
0
引用数:
0
h-index:
0
机构:
Seattle Childrens Hosp, Div Med Genet, Seattle, WA USA
Seattle Childrens Hosp, Div Med Genet, Seattle, WA USA
Hale, S.
[
1
]
Murray, M.
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Washington, Seattle, WA 98195 USA
Seattle Childrens Hosp, Div Med Genet, Seattle, WA USA
Murray, M.
[
2
]
Horslen, S.
论文数:
0
引用数:
0
h-index:
0
机构:
Seattle Childrens Hosp, Div Gastroenterol, Seattle, WA USA
Seattle Childrens Hosp, Div Med Genet, Seattle, WA USA
Horslen, S.
[
3
]
Weiss, A.
论文数:
0
引用数:
0
h-index:
0
机构:
Seattle Childrens Hosp, Dept Opthalmol, Seattle, WA USA
Seattle Childrens Hosp, Div Med Genet, Seattle, WA USA
Weiss, A.
[
4
]
Merritt, J. L., II
论文数:
0
引用数:
0
h-index:
0
机构:
Seattle Childrens Hosp, Div Med Genet, Seattle, WA USA
Seattle Childrens Hosp, Div Med Genet, Seattle, WA USA
Merritt, J. L., II
[
1
]
Hahn, S.
论文数:
0
引用数:
0
h-index:
0
机构:
Seattle Childrens Hosp, Div Med Genet, Seattle, WA USA
Seattle Childrens Hosp, Div Med Genet, Seattle, WA USA
Hahn, S.
[
1
]
机构
:
[1]
Seattle Childrens Hosp, Div Med Genet, Seattle, WA USA
[2]
Univ Washington, Seattle, WA 98195 USA
[3]
Seattle Childrens Hosp, Div Gastroenterol, Seattle, WA USA
[4]
Seattle Childrens Hosp, Dept Opthalmol, Seattle, WA USA
来源
:
MOLECULAR GENETICS AND METABOLISM
|
2009年
/ 98卷
/ 1-2期
关键词
:
D O I
:
暂无
中图分类号
:
R5 [内科学];
学科分类号
:
1002 ;
100201 ;
摘要
:
432
引用
收藏
页码:78 / 78
页数:1
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Molecular Medicine,
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Germain, DP
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Hop Europeen Georges Pompidou, Dept Genet, F-75015 Paris, France
Germain, DP
Shabbeer, J
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Hop Europeen Georges Pompidou, Dept Genet, F-75015 Paris, France
Shabbeer, J
Cotigny, S
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0
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0
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Hop Europeen Georges Pompidou, Dept Genet, F-75015 Paris, France
Cotigny, S
Desnick, RJ
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Hop Europeen Georges Pompidou, Dept Genet, F-75015 Paris, France
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MOLECULAR MEDICINE,
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不详
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Genotype-phenotype correlations in Gorlin syndrome
Evans, G.
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Christie Hosp, Manchester, Lancs, England
Evans, G.
Oudit, D.
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Christie Hosp, Manchester, Lancs, England
Christie Hosp, Manchester, Lancs, England
Oudit, D.
Smith, M. J.
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0
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Christie Hosp, Manchester, Lancs, England
Smith, M. J.
Rutkowski, D.
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Salford Royal Hosp, Salford, Lancs, England
Christie Hosp, Manchester, Lancs, England
Rutkowski, D.
Roberts, S. A.
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Christie Hosp, Manchester, Lancs, England
Roberts, S. A.
Allan, E.
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Christie Hosp, Manchester, Lancs, England
Christie Hosp, Manchester, Lancs, England
Allan, E.
Newman, W. G.
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0
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Christie Hosp, Manchester, Lancs, England
Newman, W. G.
Lear, J.
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Univ Childrens Hosp, Inst Human Genet, Dept Pediat Endocrinol, Erlangen, Germany
Zenker, M
Buheitel, G
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Univ Childrens Hosp, Inst Human Genet, Dept Pediat Endocrinol, Erlangen, Germany
Buheitel, G
Rauch, R
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0
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Univ Childrens Hosp, Inst Human Genet, Dept Pediat Endocrinol, Erlangen, Germany
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Koenig, R
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Univ Childrens Hosp, Inst Human Genet, Dept Pediat Endocrinol, Erlangen, Germany
Koenig, R
Bosse, K
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0
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Univ Childrens Hosp, Inst Human Genet, Dept Pediat Endocrinol, Erlangen, Germany
Bosse, K
Kress, W
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Univ Childrens Hosp, Inst Human Genet, Dept Pediat Endocrinol, Erlangen, Germany
Kress, W
Tietze, HU
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Univ Childrens Hosp, Inst Human Genet, Dept Pediat Endocrinol, Erlangen, Germany
Tietze, HU
Doerr, HG
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Univ Childrens Hosp, Inst Human Genet, Dept Pediat Endocrinol, Erlangen, Germany
Doerr, HG
Hofbeck, M
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Univ Childrens Hosp, Inst Human Genet, Dept Pediat Endocrinol, Erlangen, Germany
Hofbeck, M
Singer, H
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Univ Childrens Hosp, Inst Human Genet, Dept Pediat Endocrinol, Erlangen, Germany
Singer, H
Reis, A
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0
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Univ Childrens Hosp, Inst Human Genet, Dept Pediat Endocrinol, Erlangen, Germany
Reis, A
Rauch, A
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0
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Univ Childrens Hosp, Inst Human Genet, Dept Pediat Endocrinol, Erlangen, Germany
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Univ Wurzburg, Biozentrum, Dept Human & Med Genet, D-97074 Wurzburg, Germany
Univ Wurzburg, Biozentrum, Dept Human & Med Genet, D-97074 Wurzburg, Germany
Neveling, Kornelia
Endt, Daniela
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0
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机构:
Univ Wurzburg, Biozentrum, Dept Human & Med Genet, D-97074 Wurzburg, Germany
Univ Wurzburg, Biozentrum, Dept Human & Med Genet, D-97074 Wurzburg, Germany
Endt, Daniela
Hoehn, Holger
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0
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Univ Wurzburg, Biozentrum, Dept Human & Med Genet, D-97074 Wurzburg, Germany
Univ Wurzburg, Biozentrum, Dept Human & Med Genet, D-97074 Wurzburg, Germany
Hoehn, Holger
Schindler, Detlev
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0
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0
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Univ Wurzburg, Biozentrum, Dept Human & Med Genet, D-97074 Wurzburg, Germany
Univ Wurzburg, Biozentrum, Dept Human & Med Genet, D-97074 Wurzburg, Germany
Schindler, Detlev
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0
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Univ Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Desai, KB
Van Quill, KR
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0
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0
h-index:
0
机构:
Univ Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Van Quill, KR
Tsai, T
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0
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0
h-index:
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Univ Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Tsai, T
Gallie, B
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0
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Univ Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
Gallie, B
O'Brien, JM
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0
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Univ Calif San Francisco, Dept Ophthalmol, San Francisco, CA 94143 USA
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INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE,
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Panicker, J.
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Bonello, M.
Ellis, R.
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Ellis, R.
Randall, A.
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Fratalia, L.
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