Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Robert A. Conte"'
Publikováno v:
Genetics and Molecular Biology, Vol 23, Iss 3, Pp 527-529 (2000)
Homologies between chromosome banding patterns and DNA sequences in the great apes and humans suggest an apparent common origin for these two lineages. The availability of DNA probes for specific regions of human chromosomes (5q31, 10q22, 13q32-33 an
Externí odkaz:
https://doaj.org/article/aacd092a76d74e7f887709c17c234b8b
Publikováno v:
Clinical Genetics. 41:82-86
Verma RS, Conte RA, Sayegh SE, Kanjilal D. The interstitial deletion of bands q33–35 of long arm of chromosome 7: a review with a new case report. Clin Genet 1992:41: 82–86. Interstitial or terminal deletion resulting in partial monosomy of vario
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c57e0d6ffd2d886f3ea4b719c6d8fd08
https://doi.org/10.1111/j.1399-0004.1992.tb03638.x
https://doi.org/10.1111/j.1399-0004.1992.tb03638.x
Publikováno v:
Clinical Genetics. 51:196-199
We report on a new case with ring chromosome 16. Initially, the cytogenetic findings with GTG-banding revealed a 46, XY, r(16)(::p13.3 q24::)/46, XY karyotype. This is the first case of r(16) co-existing with a normal cell line with minimal clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1655eb791b03f67149ae5c0957a4523
https://doi.org/10.1111/j.1399-0004.1997.tb02452.x
https://doi.org/10.1111/j.1399-0004.1997.tb02452.x
Publikováno v:
Clinical Genetics. 50:103-105
Fortuitously, within a 1-month period, we were referred two individuals for routine cytogenetic amniocenteses involving one chromosome 21 from each patient, which had apparently lost the entire short arm and a major portion of the centromeric alphoid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff794450921423254daea2feb8709e1f
https://doi.org/10.1111/j.1399-0004.1996.tb02358.x
https://doi.org/10.1111/j.1399-0004.1996.tb02358.x
Publikováno v:
Genetica. 105:31-34
Relative phylogenetic divergence of the members of the Pongidae family has been based on genetic evidence. The recent isolation of subtelomeric probes specific for human (HSA) chromosomes 1q, 11p, 13q, and 16q has prompted us to cross hybridize these
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbb04cad5714cef683c4ad5c3a6155c9
https://doi.org/10.1023/a:1003521806089
https://doi.org/10.1023/a:1003521806089
Publikováno v:
Heredity. 81:10-13
Almost a quarter of a century ago, the banding patterns of human and other higher primate chromosomes were compared, creating a barrage of speculation. Consequently, a number of approaches have been used to understand human descent. Chromosome modifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fc05b01f1aae110e03e1c225305b558
https://doi.org/10.1046/j.1365-2540.1998.00362.x
https://doi.org/10.1046/j.1365-2540.1998.00362.x
Publikováno v:
Gynecologic and Obstetric Investigation. 45:12-15
Chromosomal mosaicism during prenatal diagnosis has been a major concern. Nondisjunctional events can lead to mosaicism in a number of ways, including failure of chromosomal pairing, failure to separate, anaphase lag and abnormal segregation. We prov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29bf17ff2d30526f37bddf0c0f7b5ef8
https://doi.org/10.1159/000009915
https://doi.org/10.1159/000009915
Publikováno v:
DNA Research. 4:249-252
Phylogenetic divergence of the members of the Pongidae family has been based on genetic evidence. The terminal repeat array (T2AG3) has lately been considered as an additional basis to analyze genomes of highly related species. The recent isolation o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::804dff288fabff852d6e0c2d298f5fb1
https://doi.org/10.1093/dnares/4.3.249
https://doi.org/10.1093/dnares/4.3.249
Publikováno v:
Human Genetics. 98:576-580
Pericentric inversions involving the secondary constriction (qh) region of chromosome 9 are considered to be normal variants. The evolutionary mechanisms and conservation of these inversions via Mendelian fashion have been investigated since the adve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f685cc8bec9cdc26c24154042b00ea8
https://doi.org/10.1007/s004390050262
https://doi.org/10.1007/s004390050262
Molecular characterization of an unusual variant of the short arm of chromosome 15 by FISH-technique
Publikováno v:
Japanese journal of human genetics. 41:307-311
One of the most frequent translocations involving the long arm of chromosome Y with autosomes is with the short arm of chromosome 15. The regions which are involved in this translocation fluoresce brightly, are highly heteromorphic and thus escape de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71739cb5e1973d394cd59fa522fb67d9
https://doi.org/10.1007/bf01913173
https://doi.org/10.1007/bf01913173