AluI-resistant chromatin of chromosome 18: classification, frequencies and implications
暂无分享,去创建一个
[1] M. Macera,et al. Identification of marker chromosomes by restriction endonucleases/Giemsa technique in neoplastic cells. , 1987, Cancer genetics and cytogenetics.
[2] R. Verma,et al. Characterization of human chromosomal constitutive heterochromatin. , 1986, Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie.
[3] R. Verma,et al. The heteromorphic marker on chromosome 18 using restriction endonuclease AluI. , 1986, American journal of human genetics.
[4] R. Verma,et al. A possible cause of non-disjunction of additional chromosome 21 in Down syndrome , 1986, Molecular and General Genetics MGG.
[5] C. Jackson-Cook,et al. Nucleolar organizer region variants as a risk factor for Down syndrome. , 1985, American journal of human genetics.
[6] R. C. Juberg,et al. Origin of nondisjunction in trisomy 21 syndrome: all studies compiled, parental age analysis, and international comparisons. , 1983, American journal of medical genetics.
[7] E. Hook,et al. Chromosomal abnormality rates at amniocentesis and in live-born infants. , 1983, JAMA.
[8] R. Phillips. New C band markers of human chromosomes: C band position variants. , 1980, Journal of medical genetics.
[9] N. Bianchi,et al. The mechanism and pattern of banding induced by restriction endonucleases in human chromosomes , 2004, Chromosoma.
[10] R. Regal,et al. The frequency of 47,+21, 47,+18, and 47,+13 at the uppermost extremes of maternal ages: results on 56,094 fetuses studied prenatally and comparisons with data on livebirths , 2004, Human Genetics.
[11] K. Jones. Heterochromatin—Molecular and structural aspects: Ram S. Verma, Cambridge University Press, 1988. £30.00/$49.50 (xv + 301 pages) ISBN 0 521 33480 2 , 1989 .
[12] R. Verma. Heterochromatin : molecular and structural aspects , 1988 .
[13] R. Verma,et al. Chromosome structure: euchromatin and heterochromatin. , 1987, International review of cytology.
[14] P. Jacobs,et al. Trisomy in man. , 1984, Annual review of genetics.
[15] R. Verma,et al. Human chromosomal heteromorphisms: nature and clinical significance. , 1980, International review of cytology.
[16] H. Lubs,et al. Human Q and C chromosomal variations: distribution and incidence. , 1975, Cytogenetics and cell genetics.