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Publikováno v:
Clinical Genetics. 13:271-277
A modification of immunoadsorbent column separation of T- and B-lymphocytes has been used to obtain karyotypable chromosome preparations. This method may be of some use in helping to gain further information about some mosaic conditions or the chromo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d8406ae18cf70c5f4e08c2a84b428c8
https://doi.org/10.1111/j.1399-0004.1978.tb01181.x
https://doi.org/10.1111/j.1399-0004.1978.tb01181.x
Autor:
Hungshu Wang, Lorraine F. Meisner, Lisa G. Shaffer, Shivanand R. Patil, Douglas W. Hershey, Lillian Y. F. Hsu, Gail Stetten, Christine M. Disteche, Fran Williams, Rodney R. Higgins, Colleen Jackson-Cook, Barbara F. Crandall, Gregory A. Mengden, Leonard J. Sciorra, Ann Leslie Zaslav, Roger P. Donahue, Elizabeth Keitges, Robert Wallerstein, Gabriel S. Khodr, Richard L. Neu, Frederick W. Luthardt, Daniel L. Van Dyke, Catherine Lee Bowen, Peter Benn, Lauren S. Jenkins, Maria Y. Rodriguez, Ming Tsung Yu, Chyi-Chyang Lin, Betty Harrison
Publikováno v:
Prenatal Diagnosis. 20:103-122
Karyotype–phenotype correlations of common trisomy mosaicism prenatally diagnosed via amniocentesis was reviewed in 305 new cases from a collaboration of North American cytogenetic laboratories. Abnormal outcome was noted in 10/25 (40%) cases of 47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::712156e319e1793d86662027c03677bc
https://doi.org/10.1002/(sici)1097-0223(200002)20:2<103::aid-pd761>3.0.co
https://doi.org/10.1002/(sici)1097-0223(200002)20:2<103::aid-pd761>3.0.co
Autor:
Mike Jaffe, Willas B. Hammond, Treena L. Arinzeh, Peter Tolias, Robert T. Dombrowski, N. Sanjeeva Murthy, Nathan D. Gallant, James A. Cooper, Benjamin R. Mintz, SunMi L. Palumbo, Wan-Ju Li, Radoslaw A. Junka, Lindsay E. Daly, Xiaojun Yu, P. Sidney Sit, Leonard J. Sciorra, Aileen Arriola, Virginie M. Aris, Shayne C. Gad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebbf32367ad89785979c7c4a4b934649
https://doi.org/10.1016/b978-1-84569-810-2.50012-2
https://doi.org/10.1016/b978-1-84569-810-2.50012-2
Publikováno v:
American Journal of Medical Genetics. 56:141-146
Using standard cytogenetic methods coupled with molecular techniques, the following karyotype mos 45,X/46,XXq+/46,X+mar (X)/47,XXq+,+mar(X), was identified in a patient with Ullrich-Turner syndrome (UTS). High-resolution banding (n = 650) of the meta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e238d081a51273fad6f36f4eefc3416a
https://doi.org/10.1002/ajmg.1320560205
https://doi.org/10.1002/ajmg.1320560205
Publikováno v:
Journal of Pediatric Surgery. 27:1376-1380
Although girls with Turner's syndrome (45,X) are not at risk for malignancy, patients with feminizing testicular syndrome with XY chromosome composition and patients with "mixed gonadal dysgenesis" are at risk for malignancy, and bilateral gonadectom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2506b652b61b299daa2629a50cae425
https://doi.org/10.1016/0022-3468(92)90180-f
https://doi.org/10.1016/0022-3468(92)90180-f
Publikováno v:
Cytogenetics and cell genetics. 95(3-4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a74ff4635d97631755bdf1722784e615
https://pubmed.ncbi.nlm.nih.gov/12063407
https://pubmed.ncbi.nlm.nih.gov/12063407
Publikováno v:
Cytogenetics and cell genetics. 95(3-4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d1ba4aeb4aeb0c6c5b93fe88f77bc5c3
https://pubmed.ncbi.nlm.nih.gov/12063408
https://pubmed.ncbi.nlm.nih.gov/12063408
Publikováno v:
Cytogenetics and cell genetics. 93(1-2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::87a1cd8f15937b25c93f3117439c5876
https://pubmed.ncbi.nlm.nih.gov/11474202
https://pubmed.ncbi.nlm.nih.gov/11474202
Autor:
R, Wallerstein, M T, Yu, R L, Neu, P, Benn, C, Lee Bowen, B, Crandall, C, Disteche, R, Donahue, B, Harrison, D, Hershey, R R, Higgins, L S, Jenkins, C, Jackson-Cook, E, Keitges, G, Khodr, C C, Lin, F W, Luthardt, L, Meisner, G, Mengden, S R, Patil, M, Rodriguez, L J, Sciorra, L G, Shaffer, G, Stetten, D L, Van Dyke, H, Wang
Publikováno v:
Prenatal diagnosis. 20(2)
Karyotype-phenotype correlations of common trisomy mosaicism prenatally diagnosed via amniocentesis was reviewed in 305 new cases from a collaboration of North American cytogenetic laboratories. Abnormal outcome was noted in 10/25 (40%) cases of 47,+
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::42f0bf1af3497b35bd445394f59453cf
https://pubmed.ncbi.nlm.nih.gov/10694683
https://pubmed.ncbi.nlm.nih.gov/10694683