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Volumn 38, Issue 3, 1997, Pages 201-204

Quantitative analysis of constitutive heterochromatin in couples with fetal wastage

Author keywords

Abortion; Heterochromatin; Spontaneous

Indexed keywords

ARTICLE; CHROMOSOME 16; CHROMOSOME BANDING PATTERN; CONSTITUTIVE HETEROCHROMATIN; CONTROLLED STUDY; EMBRYO DEVELOPMENT; FETUS MALFORMATION; FETUS WASTAGE; HUMAN; IMMUNE DEFICIENCY; KARYOTYPE; METAPHASE CHROMOSOME; PHENOTYPE; PREGNANCY COMPLICATION; PRIORITY JOURNAL; REPRODUCTION; SPONTANEOUS ABORTION; STILLBIRTH; T LYMPHOCYTE; Y CHROMOSOME;

EID: 0343052576     PISSN: 87558920     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1600-0897.1997.tb00299.x     Document Type: Article
Times cited : (15)

References (13)
  • 1
    • 0025241916 scopus 로고
    • Kinetochore formation in experimentally undercondensed chromosomes
    • Haaf T, Schmid M: Kinetochore formation in experimentally undercondensed chromosomes. Hum Genet 1990; 84:535-538.
    • (1990) Hum Genet , vol.84 , pp. 535-538
    • Haaf, T.1    Schmid, M.2
  • 2
    • 0020308904 scopus 로고
    • Minor chromosomal variants and major chromosomal abnormalities in couples with recurrent abortion
    • Blumberg BD, Shulkin JD, Rotter JI, Mohandas T, Kaback MM: Minor chromosomal variants and major chromosomal abnormalities in couples with recurrent abortion. Am J Hum Genet 1982; 34:948-960.
    • (1982) Am J Hum Genet , vol.34 , pp. 948-960
    • Blumberg, B.D.1    Shulkin, J.D.2    Rotter, J.I.3    Mohandas, T.4    Kaback, M.M.5
  • 3
    • 0020559089 scopus 로고
    • C heterochromatin variation in couples with recurrent early abortions
    • Maes A, Staessen C, Hens L, et al.: C heterochromatin variation in couples with recurrent early abortions. J Med Genet 1983; 20:350-356.
    • (1983) J Med Genet , vol.20 , pp. 350-356
    • Maes, A.1    Staessen, C.2    Hens, L.3
  • 4
    • 0016704081 scopus 로고
    • A possible function of constitutive heterochromatin: The bodyguard hypothesis
    • Hsu TC: A possible function of constitutive heterochromatin: The bodyguard hypothesis. Genetics 1975; 79(Suppl): 137-150.
    • (1975) Genetics , vol.79 , Issue.SUPPL. , pp. 137-150
    • Hsu, T.C.1
  • 5
    • 0020638950 scopus 로고
    • Heterochromatic regions on chromosomes 1, 9, 16, and Y in children with some disturbances occuring during embryo development
    • Podugolnikova OA, Blumina MG: Heterochromatic regions on chromosomes 1, 9, 16, and Y in children with some disturbances occuring during embryo development. Hum Genet 1983; 63:183-188.
    • (1983) Hum Genet , vol.63 , pp. 183-188
    • Podugolnikova, O.A.1    Blumina, M.G.2
  • 6
    • 0021684338 scopus 로고
    • Relationship of the variability of the heterochromatic regions of chromosomes 1, 9, 16, and Y to some anthropometric characteristics in children with embryopathies of unknown etiology and in children with Down syndrome
    • Podugolnikova OA, Grigorjeva NM, Blumina MG: Relationship of the variability of the heterochromatic regions of chromosomes 1, 9, 16, and Y to some anthropometric characteristics in children with embryopathies of unknown etiology and in children with Down syndrome. Hum Genet 1984; 68:254-257.
    • (1984) Hum Genet , vol.68 , pp. 254-257
    • Podugolnikova, O.A.1    Grigorjeva, N.M.2    Blumina, M.G.3
  • 7
    • 0025612383 scopus 로고
    • Quantitative analysis of constitutive heterochromatin of chromosomes 1, 9 and 16 in children with congenital abnormalities
    • PetkoviF I: Quantitative analysis of constitutive heterochromatin of chromosomes 1, 9 and 16 in children with congenital abnormalities. Period Biol 1990; 92:335-339.
    • (1990) Period Biol , vol.92 , pp. 335-339
    • Petkovif, I.1
  • 8
    • 0028010158 scopus 로고
    • Interactive computer-assisted analysis of chromosome 1 colocalization with nucleoli
    • Léger I, Guillaud M, Krief B, Brugal G: Interactive computer-assisted analysis of chromosome 1 colocalization with nucleoli. Cytometry 1994; 16:313-323.
    • (1994) Cytometry , vol.16 , pp. 313-323
    • Léger, I.1    Guillaud, M.2    Krief, B.3    Brugal, G.4
  • 9
    • 0022644043 scopus 로고
    • Molecular hybridization to meiotic chromosomes in man reveals sequence arrangement on the No. 9 chromosome and provide clues to the nature of "parameres"
    • Mitchell AR, Ambros P, McBeath S, Chandley AC: Molecular hybridization to meiotic chromosomes in man reveals sequence arrangement on the No. 9 chromosome and provide clues to the nature of "parameres." Cytogenet Cell Genet 1986; 41:89-95.
    • (1986) Cytogenet Cell Genet , vol.41 , pp. 89-95
    • Mitchell, A.R.1    Ambros, P.2    McBeath, S.3    Chandley, A.C.4
  • 11
    • 0027267470 scopus 로고
    • Evidence of chromosome 9 origin of the euchromatic variant band within 9qh
    • Hoo JJ, Szego K, Wong P, Roland B: Evidence of chromosome 9 origin of the euchromatic variant band within 9qh. Clin Genet 1993; 43:309-311.
    • (1993) Clin Genet , vol.43 , pp. 309-311
    • Hoo, J.J.1    Szego, K.2    Wong, P.3    Roland, B.4
  • 12
    • 0020370628 scopus 로고
    • Aspects of evaluation, significance, and evolution of human C-band heteromorphism
    • Erdtmann B: Aspects of evaluation, significance, and evolution of human C-band heteromorphism. Hum Genet 1982;61:281-294.
    • (1982) Hum Genet , vol.61 , pp. 281-294
    • Erdtmann, B.1
  • 13
    • 44049117443 scopus 로고
    • Molecular characterization of the smallest secondary constriction region (qh) of human chromosome 16
    • Verma RS, Luke S, Mathews T, Conte RA: Molecular characterization of the smallest secondary constriction region (qh) of human chromosome 16. Genet Anal Tech Appl 1992;9:140-142.
    • (1992) Genet Anal Tech Appl , vol.9 , pp. 140-142
    • Verma, R.S.1    Luke, S.2    Mathews, T.3    Conte, R.A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.