Zobrazeno 1 - 10
of 57
pro vyhledávání: '"McGillivray, B C"'
Autor:
Warburton, D., Lange, K., Carpenter, N. J., Erdman, C., Rao, K. W., Barlow, G. M., Lott, I. T., Tirosh-Wagner, T., Snyder, M., Doran, E., Kasowski, M., Korbel, J. O., Chen, X.-N., Grubert, F., Gao, M. C., Cohen, M. Y., Van Riper, A. J., Sobel, E. M., Pettenati, M. J., Gerstein, M. B., Lewin, S. O., Urban, A. E., Shaffer, L. G., Shohat, M., Pueschel, S. M., Moeschler, J. B., Falik-Zaccai, T., Dai, L., Weissman, S., McGillivray, B. C., Aylsworth, A. S., Clark, R. D.
Down syndrome (DS), or trisomy 21, is a common disorder associated with several complex clinical phenotypes. Although several hypotheses have been put forward, it is unclear as to whether particular gene loci on chromosome 21 (HSA21) are sufficient t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d04a5f646d4a958b37349f50e78a6c30
Akademický článek
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Publikováno v:
Prenatal Diagnosis; Oct1988, Vol. 8 Issue 8, p577-584, 8p
Publikováno v:
Prenatal Diagnosis; May1985, Vol. 5 Issue 3, p191-198, 8p
Autor:
Drumheller, T, McGillivray, B C, Behrner, D, MacLeod, P, McFadden, D E, Roberson, J, Venditti, C, Chorney, K, Chorney, M, Smith, D I
Publikováno v:
Journal of Medical Genetics; Oct1996, Vol. 33 Issue 10, p842-847, 6p, 1 Black and White Photograph, 3 Charts, 1 Graph
Autor:
McGillivray, B C, Hall, J G
Publikováno v:
Pediatrics in Review; Dec1987, Vol. 9 Issue 6, p197-202, 6p
Publikováno v:
Mathematical Biosciences; 2001, Vol. 171 Issue: 1 p99-111, 13p
Autor:
Gessler, Manfred, Thomas, G. H., Couillin, P., Junien, C., McGillivray, B. C., Hayden, M., Jaschek, G., Bruns, G. A.
The WAGR (Wilms tumor, aniridia, genitourinary anomalies, and mental retardation) region has been assigned to chromosome 11p13 on the basis of overlapping constitutional deletions found in affected individuals. We have utilized 31 DNA probes which ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______713::ea135d671476be3e471c33283f700b96
https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-59255
https://nbn-resolving.org/urn:nbn:de:bvb:20-opus-59255
Cytogenetic analysis of 14 placentas from live newborn infants or from terminated pregnancies with trisomies 13 and 18 revealed that all were mosaic. The mosaicism was confined to the cytotrophoblast and not detected in villous stroma, chorionic plat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fddfdb5ca281c76966c4f5042aaf2425
https://europepmc.org/articles/PMC1715446/
https://europepmc.org/articles/PMC1715446/
Autor:
Farrell, K., McGillivray, B. C.
Publikováno v:
Developmental Medicine & Child Neurology; 1983, Vol. 25 Issue 5, p648-650, 3p