SCOPUS 정보 검색 플랫폼

Human Mutation

Volumn 32, Issue 4, 2011, Pages 486-490

Exploring the functional consequences of genomic variation: The 2010 Human Genome Variation Society Scientific Meeting

(1) Oetting, William S a

a UNIVERSITY OF MINNESOTA (United States)

Author keywords

Databases; Functionality; HGVS; Meeting report; Prediction; Variation

Indexed keywords

ALGORITHM; COMPUTER ANALYSIS; CONFERENCE PAPER; EXOME; GENE FUNCTION; GENE MUTATION; GENE SEQUENCE; GENETIC VARIABILITY; HUMAN; MEDICAL SOCIETY; PREDICTION; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

ALGORITHMS; GENETIC VARIATION; GENOME, HUMAN; HUMANS; SEQUENCE ANALYSIS, DNA;

EID: 79952752993 PISSN: 10597794 EISSN: 10981004 Source Type: Journal
DOI: 10.1002/humu.21443 Document Type: Conference Paper

Times cited : (5)

References (6)

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3
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- De novo mutations of SETBP1 cause Schinzel-Giedion syndrome
- Hoischen A, van Bon BW, Gilissen C, Arts P, van Lier B, Steehouwer M, de Vries P, de Reuver R, Wieskamp N, Mortier G, Devriendt K, Amorim MZ, Revencu N, Kidd A, Barbosa M, Turner A, Smith J, Oley C, Henderson A, Hayes IM, Thompson EM, Brunner HG, de Vries BB, Veltman JA. 2010. De novo mutations of SETBP1 cause Schinzel-Giedion syndrome. Nat Genet 42:483-485.
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- Hoischen, A.¹ van Bon, B.W.² Gilissen, C.³ Arts, P.⁴ van Lier, B.⁵ Steehouwer, M.⁶ de Vries, P.⁷ de Reuver, R.⁸ Wieskamp, N.⁹ Mortier, G.¹⁰ Devriendt, K.¹¹ Amorim, M.Z.¹² Revencu, N.¹³ Kidd, A.¹⁴ Barbosa, M.¹⁵ Turner, A.¹⁶ Smith, J.¹⁷ Oley, C.¹⁸ Henderson, A.¹⁹ Hayes, I.M.²⁰ more..

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- Yoshida, M.¹ Takahashi, Y.² Koike, A.³ Fukuda, Y.⁴ Goto, J.⁵ Tsuji, S.⁶

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.