Zobrazeno 1 - 10
of 15
pro vyhledávání: '"M. R. Creasy"'
Autor:
M. R. Creasy
Publikováno v:
Developmental Medicine & Child Neurology. 18:811-816
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6881cb2b54a41a8e982fa261eb084c70
https://doi.org/10.1111/j.1469-8749.1976.tb04241.x
https://doi.org/10.1111/j.1469-8749.1976.tb04241.x
Publikováno v:
Clinical Genetics. 9:15-19
An abortus with a primary trisomy 21 cell line and a cell line with a translocation between a chromosome 2 and two No. 21's is described. Both parents were chromosomally normal. Some implications of the interchange are discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93c817cdb22cccc807cedd8133d114fb
https://doi.org/10.1111/j.1399-0004.1976.tb01544.x
https://doi.org/10.1111/j.1399-0004.1976.tb01544.x
Publikováno v:
Journal of Clinical Pathology. 49:638-641
AIMS: To survey the diagnostic service provided by UK laboratories for the culture of solid tissue samples (excluding tumours) and in particular to examine the variation in culture success rates and the problems of maternal cell overgrowth. METHODS:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12f7ab4ebe2b5ee646dc3470d7d684c6
https://doi.org/10.1136/jcp.49.8.638
https://doi.org/10.1136/jcp.49.8.638
Autor:
M. R. Creasy, J. A. Crolla
Publikováno v:
Clinical Genetics. 19:481-482
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f92eca7e2c66ce3c396b433cc13eb7e
https://doi.org/10.1111/j.1399-0004.1981.tb02068.x
https://doi.org/10.1111/j.1399-0004.1981.tb02068.x
Autor:
P. A. Farndon, J. L. Watt, S. M. Bowser-Riley, M. R. Creasy, M. J. Griffiths, R. A. Johnson, D. A. G. Thomson, K. E. Martin, S. A. Larkins
Publikováno v:
Journal of Medical Genetics. 25:326-331
Double translocation heterozygotes are rare, but need not necessarily pose more of a counselling problem than single reciprocal translocation heterozygotes. Nine cases of double translocation are presented, together with a review of the few reports p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::353c5858bd01656116f06d973254a75b
https://doi.org/10.1136/jmg.25.5.326
https://doi.org/10.1136/jmg.25.5.326
Publikováno v:
BJOG: An International Journal of Obstetrics and Gynaecology. 83:621-627
Summary The effect is described of maternal factors on the proportion of fetal chromosomal anomalies in a series of 2620 spontaneous abortions, of which 992 specimens were karyotyped. Maternal age was the most important factor associated with a rise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2e9c33a6d6e76ab5a0ef4b42deda6c6
https://doi.org/10.1111/j.1471-0528.1976.tb00899.x
https://doi.org/10.1111/j.1471-0528.1976.tb00899.x
Publikováno v:
Journal of Medical Genetics. 20:81-85
The male antifertility agent Gossypol did not affect the level of traditional chromosome breakage or number of micronuclei in 66-hour lymphocyte cultures at concentrations up to 40 micrograms/ml. It did increase the frequency of SCE slightly, althoug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5790ee93f789cd7757ee54d1ac2ed10d
https://doi.org/10.1136/jmg.20.2.81
https://doi.org/10.1136/jmg.20.2.81
Autor:
M R Creasy, E D Alberman
Publikováno v:
Journal of Medical Genetics. 14:313-315
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1958756cef8983516674ee23763a76a8
https://doi.org/10.1136/jmg.14.5.313
https://doi.org/10.1136/jmg.14.5.313
Publikováno v:
Orvosi hetilap. 128(46)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::88b810751862ecb98a3552408da37153
https://pubmed.ncbi.nlm.nih.gov/3684260
https://pubmed.ncbi.nlm.nih.gov/3684260
Publikováno v:
Humangenetik. 24(4)
A spontaneous abortion with an unbalanced translocation involving chromosomes 3, 4 and 14 is described. The mother and grandmother of the abortus were balanced carriers of the condition. A marker 9 was also segregating in the family.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5ed2348fa5c6015bd72887a50159ff3
https://pubmed.ncbi.nlm.nih.gov/4140839
https://pubmed.ncbi.nlm.nih.gov/4140839