Zobrazeno 1 - 10
of 19
pro vyhledávání: '"J. M. Rary"'
Publikováno v:
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 152:39-47
The peripheral lymphocytes from 7 patients affected with ataxia telangiectasia (AT) were found to be about twice as sensitive to the induction of chromatid-type aberrations by X-rays administered during the G2 phase of the cell cycle as cells from no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab13dd5853148ab3b5c785827967d143
https://doi.org/10.1016/0027-5107(85)90044-2
https://doi.org/10.1016/0027-5107(85)90044-2
Publikováno v:
Journal of Heredity. 65:209-212
165 prenatal cytogenetic analyses are reported. The culture and Giemsa or quinacrine mustard (QM) staining processes are described. Karyotypes from both Giemsa and QM metaphases were analyzed. The main indications for amniocentesis were: 1)previous c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cb79557f22a7b438d6ab78da666bd7a
https://doi.org/10.1093/oxfordjournals.jhered.a108505
https://doi.org/10.1093/oxfordjournals.jhered.a108505
Autor:
W. R. Breg, O.J. Miller, J M Rary, Samuel H. Boyer, Stephen S. Wachtel, L. M. Kunkel, H W Jones, Kirby D. Smith, D S Borgaonkar
Publikováno v:
Proceedings of the National Academy of Sciences. 74:1245-1249
A number of individuals with aberrant Y chromosomes have been tested for the presence of Y-chromosome-specific reiterated DNA. These studies locate Y-chromosome-specific reiterated sequences on the long arm of the Y chromosome. Correlation with pheno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e3b4feb9631f2ba2f8cc23a7942d0af
https://doi.org/10.1073/pnas.74.3.1245
https://doi.org/10.1073/pnas.74.3.1245
Publikováno v:
Journal of Heredity. 68:75-80
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f2080f9a5d0235e74ed984d1e8658ae
https://doi.org/10.1093/oxfordjournals.jhered.a108794
https://doi.org/10.1093/oxfordjournals.jhered.a108794
Publikováno v:
Journal of Heredity. 59:201-204
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e5794a27b8324ceeb85b8ee44555b2bc
https://doi.org/10.1093/oxfordjournals.jhered.a107689
https://doi.org/10.1093/oxfordjournals.jhered.a107689
Publikováno v:
International Journal of Gynecology & Obstetrics. 20:261-263
The testis from two 47XXY fetuses (20 weeks) revealed histologic features not dissimilar from that observed in a normal 46XY fetus of similar gestational age. These findings support the observation that the loss of germ cells in patients with Klinefe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcbdc79347e80974d6f3c85f8a2f9be1
https://doi.org/10.1016/0020-7292(82)90052-2
https://doi.org/10.1016/0020-7292(82)90052-2
Bloom's syndrome is characterized cytogenetically by increased frequencies of chromosomal aberrations and sister chromatid exchanges. We have earlier suggested that these increases are due to the endogenous production of an agent(s) capable of damagi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::534ac49313dc7cdb9d0ad5523976654d
https://doi.org/10.1016/b978-0-12-322650-1.50129-6
https://doi.org/10.1016/b978-0-12-322650-1.50129-6
Publikováno v:
Birth defects original article series. 14(6C)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1fdcc308361b1b4a45eee83c77d29473
https://pubmed.ncbi.nlm.nih.gov/569516
https://pubmed.ncbi.nlm.nih.gov/569516
Publikováno v:
The Journal of heredity. 74(6)
This paper reports the identification of a carrier of two different balanced chromosomal translocations (45,XX,-13,-14, + t(13q;14q), t(6;8) (p11;p12]. Ascertainment occurred during family studies following prenatal diagnosis performed because of adv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f14feb91c2d529a584da618965457341
https://pubmed.ncbi.nlm.nih.gov/6643986
https://pubmed.ncbi.nlm.nih.gov/6643986
Publikováno v:
Nature. 273(5663)
BLOOM'S syndrome (BS) is a rare, autosomal recessive human disorder, characterised by growth retardation, sunlight-induced facial skin eruptions, low immunological competence and a high incidence of cancer1–4. Lymphocytes, and to a lesser extent, f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ebca6c8fc42c109925d56c1327ae4e67
https://pubmed.ncbi.nlm.nih.gov/661962
https://pubmed.ncbi.nlm.nih.gov/661962