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Volumn 107, Issue 8, 2000, Pages 969-972

Pregnancy outcome in carriers of fragile X

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BLEEDING; CONTROLLED STUDY; FEMALE; FETUS DEATH; FETUS DISTRESS; FRAGILE X SYNDROME; GENETIC COUNSELING; HETEROZYGOTE; HUMAN; MAJOR CLINICAL STUDY; PREECLAMPSIA; PREGNANCY COMPLICATION; PREMATURITY; PRIORITY JOURNAL; SMALL FOR DATE INFANT;

EID: 0033943162     PISSN: 14700328     EISSN: 14710528     Source Type: Journal    
DOI: 10.1111/j.1471-0528.2000.tb10398.x     Document Type: Article
Times cited : (7)

References (14)
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    • (1991) Diagnosis, Treatment, and Research , pp. 69-86
    • Sherman, S.1
  • 2
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  • 4
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    • Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile × syndrome
    • Verkerk AJMH, Pieretti M, Sutcliffe J et al. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile × syndrome. Cell 1991; 65: 905–914.
    • (1991) Cell , vol.65 , pp. 905-914
    • Verkerk, A.J.M.H.1    Pieretti, M.2    Sutcliffe, J.3
  • 5
    • 0026345716 scopus 로고
    • Fragile-X: A polymorphic and highly mutable CGG repeat in the FMR-1 gene
    • Fu Y-H, Kuhl DPA, Pizzutti A et al. Fragile-X: a polymorphic and highly mutable CGG repeat in the FMR-1 gene. Cell 1991; 67: 1047–1058.
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    • Fu, Y.-H.1    Kuhl, D.P.A.2    Pizzutti, A.3
  • 6
    • 0028197078 scopus 로고
    • Frequency and stability of the fragile X premutation
    • Reiss AL, Kazazian H Jr, Krebs CM et al. Frequency and stability of the fragile X premutation. Hum Mol Genet 1994; 3: 393–398.
    • (1994) Hum Mol Genet , vol.3 , pp. 393-398
    • Reiss, A.L.1    Kazazian, H.2    Krebs, C.M.3
  • 7
    • 0028799833 scopus 로고
    • Prevalence of carriers of pre-mutation size alleles of the FMR1 gene and implications for the population genetics of the fragile X syndrome
    • Rousseau F, Rouillard P, Morel ML, Khandjian EW, Morgan K. Prevalence of carriers of pre-mutation size alleles of the FMR1 gene and implications for the population genetics of the fragile X syndrome. Am J Hum Genet 1995; 57: 1006–1018.
    • (1995) Am J Hum Genet , vol.57 , pp. 1006-1018
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  • 8
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    • Fragile-X carrier females: Evidence for a distinct psychopathological phenotype
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  • 9
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    • A study of the physical behavioural, and medical phenotype, including anthropometric measures, of females with fragile X syndrome
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  • 10
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    • Obstetrical and gynaecological complications in fragile X carriers: A multicenter study
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  • 11
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  • 12
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  • 14
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    • Carrier diagnosis of the fragile X syndrome—a challenge in antenatal clinics
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    • Ryynänen, M.1    Kirkinen, P.2    Mannermaa, A.3    Saarikoski, S.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.