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Volumn 30, Issue 1-2, 1988, Pages 485-491

A non-syndromal form of X-linked mental retardation (XLMR) is linked to DXS14

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME XQ; CLINICAL ARTICLE; FAMILY STUDY; GENETIC DISORDER; GENETIC ENGINEERING; GENETIC LINKAGE; HEREDITY; HUMAN; MALE; MENTAL DEFICIENCY; PEDIGREE; PRIORITY JOURNAL; X CHROMOSOME RECESSIVE INHERITANCE;

EID: 0023766711     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1320300151     Document Type: Article
Times cited : (43)

References (9)
  • 1
    • 0021592933 scopus 로고
    • Linkage analysis of X‐linked mental retardation with and without fragile‐X using Factor IX gene probe
    • Choo KH, George D, Filby G, Halliday JL, Leversha M, Webb G, Danks DM [ 1984 ]: Linkage analysis of X‐linked mental retardation with and without fragile‐X using Factor IX gene probe. Lancet ii: 349.
    • (1984) Lancet , vol.ii , pp. 349
    • Choo, KH1    George, D2    Filby, G3    Halliday, JL4    Leversha, M5    Webb, G6    Danks, DM7
  • 2
    • 85068950077 scopus 로고
    • Report of the committee on methods of linkage analysis and reporting. 8th International Workshop on Human Gene Mapping
    • Conneally PM, Edwards JH, Kidd KK, Lalouel JM, Morton NE, Ott J, White R (1985): Report of the committee on methods of linkage analysis and reporting. 8th International Workshop on Human Gene Mapping. Cytogenet Cell Genet 40: 356–359.
    • (1985) Cytogenet Cell Genet , vol.40 , pp. 356-359
    • Conneally, PM1    Edwards, JH2    Kidd, KK3    Lalouel, JM4    Morton, NE5    Ott, J6    White, R7
  • 3
    • 0019193212 scopus 로고
    • Non‐specific X‐linked mental retardation II: The frequency in British Columbia
    • Herbst DS, Miller JR (1980): Non‐specific X‐linked mental retardation II: The frequency in British Columbia. Am J Med Genet 7: 461–469.
    • (1980) Am J Med Genet , vol.7 , pp. 461-469
    • Herbst, DS1    Miller, JR2
  • 5
    • 0023212670 scopus 로고
    • Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14
    • Mulley JC, Gedeon AK, Thorn KA, Bates LJ, Sutherland GR (1987): Linkage and genetic counselling for the fragile X using DNA probes 52A, F9, DX13, and ST14. Am J Med Genet 27: 435–448.
    • (1987) Am J Med Genet , vol.27 , pp. 435-448
    • Mulley, JC1    Gedeon, AK2    Thorn, KA3    Bates, LJ4    Sutherland, GR5
  • 6
    • 0016302483 scopus 로고
    • Estimation of the recombination fraction in human pedigrees: Efficient computation of the likelihood for human linkage studies
    • Ott J (1974): Estimation of the recombination fraction in human pedigrees: Efficient computation of the likelihood for human linkage studies. Am J Hum Genet 26: 588–597.
    • (1974) Am J Hum Genet , vol.26 , pp. 588-597
    • Ott, J1
  • 7
    • 0003555486 scopus 로고
    • Fragile Sites on Human Chromosomes
    • Sutherland GR, Hecht F (1985): “ Fragile Sites on Human Chromosomes.” New York: Oxford University Press.
    • (1985)
    • Sutherland, GR1    Hecht, F2
  • 8
    • 0015012442 scopus 로고
    • X‐linked mental retardation without physical abnormality: Renpenning's syndrome
    • Turner G, Turner B, Collins E (1971): X‐linked mental retardation without physical abnormality: Renpenning's syndrome. Dev Med Child Neurol 13: 71–78.
    • (1971) Dev Med Child Neurol , vol.13 , pp. 71-78
    • Turner, G1    Turner, B2    Collins, E3
  • 9
    • 0022201820 scopus 로고
    • Report of the committee on human gene mapping by recombinant DNA techniques. 8th International Workshop on Human Gene Mapping
    • Willard HF, Skolnick MH, Pearson PL, Mandel JL (1985): Report of the committee on human gene mapping by recombinant DNA techniques. 8th International Workshop on Human Gene Mapping. Cytogenet Cell Genet 40: 360–489.
    • (1985) Cytogenet Cell Genet , vol.40 , pp. 360-489
    • Willard, HF1    Skolnick, MH2    Pearson, PL3    Mandel, JL4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.