SCOPUS 정보 검색 플랫폼

Volumn 59, Issue 3, 1996, Pages 540-546

Decrease in the CGG(n) trinucleotide repeat mutation of the fragile X syndrome to normal size range during paternal transmission

(3) Väisänen, Marja Leena a Haataja, Ritva a,b Leisti, Jaakko a

a OULU UNIVERSITY HOSPITAL (Finland)

b UNIVERSITY OF OULU (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

TRINUCLEOTIDE; FMR1 PROTEIN, HUMAN; FRAGILE X MENTAL RETARDATION PROTEIN; NERVE PROTEIN; RNA BINDING PROTEIN;

ALLELE; ARTICLE; FRAGILE X SYNDROME; GERM LINE; HUMAN; HUMAN CELL; HUMAN TISSUE; MAJOR CLINICAL STUDY; MENTAL DEFICIENCY; MOSAICISM; NUCLEOTIDE REPEAT; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SEQUENCE ANALYSIS; SOUTHERN BLOTTING; FATHER; FEMALE; GENETIC MARKER; GENETICS; MALE; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE; TRINUCLEOTIDE REPEAT; X CHROMOSOME;

BASE SEQUENCE; DNA MUTATIONAL ANALYSIS; FATHERS; FEMALE; FRAGILE X MENTAL RETARDATION PROTEIN; FRAGILE X SYNDROME; GENETIC MARKERS; HUMANS; MALE; MOLECULAR SEQUENCE DATA; MUTATION; NERVE TISSUE PROTEINS; PEDIGREE; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; RNA-BINDING PROTEINS; TRINUCLEOTIDE REPEATS; X CHROMOSOME;

EID: 0029664941 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: None Document Type: Article

Times cited : (17)

References (5)

1
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- Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy
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2
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- New alleles at microsatellite loci in CEPH families mainly arise from somatic mutations in the lymphoblastoid cell lines
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- Banchs, I.¹ Bosch, A.² Guimerà, J.³ Lázaro, C.⁴ Puig, A.⁵ Estivill, X.⁶

3
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- Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy
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- (1992) Hum Mol Genet , vol.1 , pp. 255-258
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4
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- Reverse mutations in fragile X syndrome
- Brown WT, Nolin S, Houck GE Jr, Zhong N, Glicksman A, Ye L, Ding X, et al (1994) Reverse mutations in fragile X syndrome. Am J Hum Genet Suppl 55:1246
- (1994) Am J Hum Genet Suppl , vol.55 , pp. 1246
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- Reverse mutation in myotonic dystrophy
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.