Results 171 to 180 of about 10,109 (209)

A de novo 6q11—q15 duplication investigated by chromosome painting

Clinical Genetics, 1994
A de novo interstitial duplication of the 6q11—q15 chromosome region, confirmed by the application of a chromosome 6 painting probe, was observed in a patient with craniofacial dymorphism, psychomotor retardation, cryptorchidism and hypospadias. Despite the publication of several cases showing partial trisomy 6q, to our knowledge the duplication of the
D, Giardino, N, Rizzi, V, Briscioli, D, Bettio   +3 more
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Endometrial polyp: Another benign tumor characterized by 12q13–q15 changes

Cancer Genetics and Cytogenetics, 1993
Clustering of aberrations to specific chromosome regions of benign tumors may indicate the location of genes related to the proliferative process. Although few endometrial polyps have been cytogenetically investigated, 6p21 band appears to be involved consistently in the chromosome changes.
VANNI, ROBERTA, Dal Cin P, Marras S, Moerman P, Andria M, Valdes E, Deprest J, Van den Berghe H.   +7 more
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Clinical features in a de novo interstitial deletion 15q13 to q15

Clinical Genetics, 1988
A boy with several dysmorphic features and suffering from mental and motor retardation was found to have a de novo interstitial deletion of chromosome 15, involving bands q13 to q15. His clinical picture is described and compared with the clinical features reported in other deletions of this chromosome, located or extending distally from the region ...
S, Autio, H, Pihko, C, Tengström
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Intravenous leiomyomatosis is characterized by a der(14)t(12;14)(q15;q24)

Genes, Chromosomes and Cancer, 2002
AbstractIntravenous leiomyomatosis (IVL) is a rare smooth‐muscle proliferation that is of special interest because of its quasi‐malignant behavior. Our finding of a specific chromosomal aberration, a der(14)t(12;14)(q15;q24), in a second case of IVL suggests that it may be characteristic of IVL.
Dal Cin, Paola, Quade, Bradley J, Neskey, David M, Kleinman, Michael S, Weremowicz, Stanislawa, Morton, Cynthia C; id_orcid 0000-0003-2198-6756   +5 more
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Translocation (10;12)(q24;q15) in a T-Cell Lymphoblastic Lymphoma with Myeloid Hyperplasia

Cancer Genetics and Cytogenetics, 1998
We present a case of childhood T-cell lymphoblastic lymphoma (T-LBL) with a translocation (10;12)(q24;q15) as a main clonal abnormality, which to our knowledge is the first reported karyotype of this malignancy. The patient's peripheral blood and bone marrow showed marked leukocytosis mostly myeloid lineage cells, at diagnosis.
K, Sano, J, Goji, Y, Kosaka, H, Nakamura, F, Nakamura, E, Tatsumi   +5 more
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Molecular analysis of a familial case of renal cell cancer and a t(3;6)(q12;q15)

Genes, Chromosomes and Cancer, 2001
AbstractWe identified a novel familial case of clear‐cell renal cancer and a t(3;6)(q12;q15). Subsequent cytogenetic and molecular analyses showed the presence of several abnormalities within tumour samples obtained from different patients. Loss of the der(3) chromosome was noted in some, but not all, of the samples. A concomitant VHL gene mutation was
Eleveld, M. J., Bodmer, D., Merkx, G., Siepman, A., Sprenger, S. H., Weterman, M. A., Ligtenberg, M. J., Kamp, J., Stapper, W., Jeuken, J. W., Smeets, D., Smits, A., Geurts van Kessel, A.   +12 more
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Molecular-cytogenetic refinement of the 12q14→q15 breakpoint region affected in uterine leiomyomas

Cytogenetics and Cell Genetics, 2008
Recent molecular and cytogenetic studies on uterine leiomyoma cell lines with aberrations in 12q14→q15 have shown that the chromosome 12 breakpoints seem to cluster in a 260-kb region designated as ULCR 12 (uterine leiomyoma cluster region of chromosome 12 breakpoints).
S, Wanschura, Y, Hennig, U, Deichert, E F, Schoenmakers, W J, Van de Ven, S, Bartnitzke, J, Bullerdiek   +6 more
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Trophoblast glycoprotein recognised by monoclonal antibody 5T4 maps to human chromosome 6q14?q15

Human Genetics, 1990
Human X rodent hybrids were stained by indirect immunofluorescence with 5T4, a murine monoclonal antibody that recognises a 72 kdalton glycoprotein expressed by human trophoblasts and a very restricted range of adult tissues; they were analysed by flow cytometry.
J M, Boyle, K H, Grzeschik, P R, Heath, J E, Morten, P L, Stern   +4 more
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MPEC 2025-Q15 : 2025 PR2

The Minor Planet Electronic Circulars contain information on unusual minor planets, routine data on comets and natural satellites, and occasional editorial announcements. They are published on behalf of Division F of the International Astronomical Union by the Minor Planet Center, Smithsonian Astrophysical Observatory, Cambridge, MA 02138, U.S.A.
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MPEC 2024-Q15 : 2024 QB

The Minor Planet Electronic Circulars contain information on unusual minor planets, routine data on comets and natural satellites, and occasional editorial announcements. They are published on behalf of Division F of the International Astronomical Union by the Minor Planet Center, Smithsonian Astrophysical Observatory, Cambridge, MA 02138, U.S.A.
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