SCOPUS 정보 검색 플랫폼

Clinical Genetics

Volumn 54, Issue 2, 1998, Pages 152-154

Polymorphic variants within the homeobox gene MSX1: A candidate gene for developmental disorders

(2) Hollway, Georgina E a Mulley, John C a

a WOMEN S AND CHILDREN S HOSPITAL (Australia)

Author keywords

Craniosynostosis; MSX1; Polymorphism

Indexed keywords

DNA;

AMINO ACID SUBSTITUTION; ARTICLE; CHROMOSOME 4P; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; DNA POLYMORPHISM; GENE DELETION; GENE FREQUENCY; GENE MAPPING; HETEROZYGOSITY; HOMEOBOX; HUMAN; MAJOR CLINICAL STUDY; NUCLEIC ACID BASE SUBSTITUTION; PRIORITY JOURNAL;

EID: 0031715996 PISSN: 00099163 EISSN: None Source Type: Journal
DOI: 10.1111/j.1399-0004.1998.tb03719.x Document Type: Article

Times cited : (3)

References (6)

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2
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- The human homeobox gene HOX7 maps to chromosome 4p16.1 and may be implicated in Wolf-Hirschhorn syndrome
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3
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- Localization of craniosynostosis Adelaide type to 4p16
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- (1995) Hum Mol Genet , vol.4 , pp. 681-683
- Hollway, G.E.¹ Phillips, H.A.² Ades, L.C.³ Haan, E.A.⁴ Mulley, J.C.⁵

4
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- A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome
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- Muenke, M.¹ Gripp, K.W.² McDonald-McGinn, D.M.³ Gaudenz, K.⁴ Whitaker, L.A.⁵ Bartlett, S.P.⁶ Markowitz, R.I.⁷ Robin, N.H.⁸ Nwokoro, N.⁹ Mulvihill, J.J.¹⁰ Losken, H.W.¹¹ Mulliken, J.B.¹² Guttmacher, A.E.¹³ Wilroy, R.S.¹⁴ Clarke, L.A.¹⁵ Hollway, G.¹⁶ Adès, L.C.¹⁷ Haan, E.A.¹⁸ Mulley, J.C.¹⁹ Cohen Jr., M.M.²⁰ more..

5
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- A human MSX1 homeodomain missense mutation causes selective tooth agenesis
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6
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- Characterization of the human HOX7 cDNA and identification of polymorphic markers
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.