Benign ovarian teratomas. An analysis of their cellular origin.
暂无分享,去创建一个
[1] J. Rastad,et al. Cytogenetical investigations in patients with primary hyperparathyroidism and multiple endocrine neoplasia type 1. , 2008, Hereditas.
[2] G. Mutter. Teratoma genetics and stem cells: a review. , 1987, Obstetrical & gynecological survey.
[3] M. Farrall,et al. Isolation of a further anonymous informative DNA sequence from chromosome seven closely linked to cystic fibrosis. , 1986, Nucleic acids research.
[4] R. Heilig,et al. Homologies between X and Y chromosomes detected by DNA probes: localisation and evolution. , 1985, Nucleic acids research.
[5] K. Ohama,et al. Origin of immature teratoma of the ovary. , 1985, American journal of obstetrics and gynecology.
[6] R. White,et al. The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[7] H. Willard,et al. PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs , 1985, The Lancet.
[8] K. E. Davies,et al. Gene for OTC: characterisation and linkage to Duchenne muscular dystrophy , 1985, Nucleic Acids Res..
[9] R. Nussbaum,et al. Two anonymous X-specific human sequences detecting restriction fragment length polymorphisms in region Xq26→qter , 1984, Somatic cell and molecular genetics.
[10] David A. Hartley,et al. A cytological map of the human X chromosome - evidence for non-random recombination , 1984, Nucleic Acids Res..
[11] J. Aldridge,et al. A strategy to reveal high-frequency RFLPs along the human X chromosome. , 1984, American journal of human genetics.
[12] S. Povey,et al. The origin of ovarian teratomas. , 1984, Journal of medical genetics.
[13] S. Povey,et al. Diverse origins of multiple ovarian teratomas in a single individual. , 1982, Proceedings of the National Academy of Sciences of the United States of America.
[14] D. Botstein,et al. Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes. , 1982, Proceedings of the National Academy of Sciences of the United States of America.
[15] J. Jonasson,et al. New staining method for the detection of sister-chromatid exchanges in BrdU-labelled chromosomes. , 1978, Journal of cell science.
[16] J. Ott,et al. Estimating distances from the centromere by means of benign ovarian teratomas in man , 1976, Annals of human genetics.
[17] H. Fox,et al. Tumours of the ovary , 1976 .
[18] E. Southern. Detection of specific sequences among DNA fragments separated by gel electrophoresis. , 1975, Journal of molecular biology.
[19] F. Hecht,et al. Parthenogenic origin of benign ovarian teratomas. , 1975, The New England journal of medicine.
[20] D. Linder,et al. Further evidence for post ‐meiotic origin of teratomas in the human female * , 1970, Annals of human genetics.
[21] T. Caspersson,et al. Differential binding of alkylating fluorochromes in human chromosomes. , 1970, Experimental cell research.
[22] D. Serr,et al. Chromosomal Studies in Tumors of Embryonic Origin , 1969, Obstetrics and gynecology.
[23] H. Jones,et al. Chromosomes of normal and neoplastic ovarian tissue. , 1968, Obstetrics and gynecology.
[24] H. Jones,et al. Chromosomes of a malignant ovarian teratoma. , 1968, American journal of obstetrics and gynecology.
[25] R B ROSEN,et al. DRUGS IN HOSPITAL. , 1965, Lancet.
[26] K. Gustavson,et al. Familial ovarian dermoid cysts. , 1988, Upsala journal of medical sciences.
[27] R. L. Miller,et al. Abstracts of workshop presentations (Part 1 of 13) , 1985 .
[28] Michael Dean,et al. A closely linked genetic marker for cystic fibrosis , 1985, Nature.
[29] F. Hecht,et al. Human benign ovarian teratomas: chromosomal and electrophoretic enzyme studies. , 1978, Birth defects original article series.