SCOPUS 정보 검색 플랫폼

Volumn 59, Issue 6, 1996, Pages 1288-1296

Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus

(12) Semina, Elena V b Datson, Nicole A b Leysens, Nancy J b Zabel, Bernhard U b Carey, John C b Bell, Graeme L b Bitoun, Pierre b Lindgren, Christine b Stevenson, Teri b Frants, Rune R b Van Ommen, Gert Jan b Murray, Jeffrey C a

a UNIVERSITY OF IOWA (United States)

b NONE

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; DNA; EPIDERMAL GROWTH FACTOR;

ARTICLE; CHROMOSOME 4Q; CLINICAL ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; EXON; GENE; GENE LOCATION; GENE TRANSLOCATION; GENETIC LINKAGE; HUMAN; HUMAN CELL; HYBRID CELL; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PULSED FIELD GEL ELECTROPHORESIS; RIEGER SYNDROME; SINGLE STRAND CONFORMATION POLYMORPHISM; YEAST ARTIFICIAL CHROMOSOME;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 4; CRANIOFACIAL ABNORMALITIES; EPIDERMAL GROWTH FACTOR; GENETIC MARKERS; GLAUCOMA; HUMANS; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SEQUENCE ANALYSIS, DNA; SYNDROME; TOOTH ABNORMALITIES; TRANSLOCATION, GENETIC; UMBILICUS;

EID: 19244364500 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (22)

References (7)

1
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- Molecular geneitcs of Rieger syndrome
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- Alward, W.L.M.¹ Murray, J.C.²

2
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- Construction of yeast artificial chromosome libraries with large inserts using fractionation by pulsed-field gel electrophoresis
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3
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- Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction
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- Orita, M.¹ Suzuki, Y.² Sekiya, T.³ Hayashi, K.⁴

4
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- A new HincII RFLP for epidermal growth factor (EGF) on chromosome 4
- Ritty TM, Murray JC (1989) A new HincII RFLP for epidermal growth factor (EGF) on chromosome 4. Nucleic Acids Res 17:5870
- (1989) Nucleic Acids Res , vol.17 , pp. 5870
- Ritty, T.M.¹ Murray, J.C.²

5
- 0027193630
- The sensitivity of single-strand conformation polymorphism analysis for the detection of single base substitutions
- Sheffield VC, Beck JS, Kwitek AE, Sandstrom DW, Stone EM (1993) The sensitivity of single-strand conformation polymorphism analysis for the detection of single base substitutions. Genomics 16:325-332
- (1993) Genomics , vol.16 , pp. 325-332
- Sheffield, V.C.¹ Beck, J.S.² Kwitek, A.E.³ Sandstrom, D.W.⁴ Stone, E.M.⁵

6
- 0027964261
- Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
- Shiang R, Thompson LM, Zhu YZ, Church DM, Fielder TJ, Bocian M, Winokur ST, et al (1994) Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia. Cell 78:335-345
- (1994) Cell , vol.78 , pp. 335-345
- Shiang, R.¹ Thompson, L.M.² Zhu, Y.Z.³ Church, D.M.⁴ Fielder, T.J.⁵ Bocian, M.⁶ Winokur, S.T.⁷

7
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- Evidence that Rieger syndrome maps to 4q25 or 4q27
- Vaux C, Sheffield L, Keith CG, Voullaire L (1992) Evidence that Rieger syndrome maps to 4q25 or 4q27. J Med Genet 29:256-258
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- Vaux, C.¹ Sheffield, L.² Keith, C.G.³ Voullaire, L.⁴

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.