Results 191 to 200 of about 10,401 (233)
t(10;12)(q24;q15): A new cytogenetic marker in hematological malignancies [PDF]
Cancer Genetics, 2022 Cytogenetic studies have played a crucial role in the discovery of genes involved in several diseases. In the field of oncohematology, cytogenetics is still necessary for the classification and prognosis of many diseases. Here we report a new recurrent chromosome translocation, t(10;12)(q24;q15), in two patients with different hematological ...
Marta Bernués +11 more
openaire +4 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Mapping of gene loci in the Q13?Q15 region of chromosome 12
Chromosome Research, 1995The gene loci CDK4, GLI, CHOP and MDM2 have been mapped to the q13-q15 region of chromosome 12. Using fluorescence in situ hybridization onto simultaneously DAPI-banded metaphase chromosomes and interphase nuclei, we have more precisely mapped and ordered these loci, together with a number of Genethon microsatellite markers.
J M Varley, E L Mitchell, J Heighway
exaly +3 more sources
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 +5 more
openaire +4 more sources
Deregulation of HMGA2 in an aggressive angiomyxoma with t(11;12)(q23;q15)
Virchows Archiv, 2006 Aggressive angiomyxoma is a soft-tissue neoplasm with a predilection for the pelvic and perineal regions and a tendency to recur locally. Cytogenetic data on this tumor type are limited to five cases, three of which showed rearrangement of chromosomal bands 12q13-15.
Francesca, Micci +3 more
openaire +3 more sources
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 +6 more
openaire +3 more sources
International Journal of Environmental Research and Public Health, 2021 Background As health literacy (HL) is hypothesized to develop throughout life, enhancement during childhood will improve HL and health during life. There are few valid, age-appropriate tools to assess children’s HL.
Marla T H Hahnraths +2 more
exaly +3 more sources
Gesundheitskompetenz im Kindesalter messen mit dem HLS-Child-Q15
, 2022 Bollweg TM, Kirchhoff S, Okan O. Gesundheitskompetenz im Kindesalter messen mit dem HLS-Child-Q15. In: Rathmann K, Dadaczynski K, Okan O, Messer M, eds. Gesundheitskompetenz. Springer Reference Pflege – Therapie – Gesundheit.
Bollweg, Torsten Michael +6 more
openaire +2 more sources
Paratesticular leiomyoma with a der(14)t(12;14)(q15;q24)
Cancer Genetics, 2011While uterine leiomyomas are among the most common and best cytogenetically characterized solid tumors, leiomyomas at other sites are rare. Only two karyotypically abnormal leiomyomas in males have been reported to date, both of them with unspecific chromosome aberrations.
Ludmila, Gorunova +2 more
openaire +2 more sources
A 6q14.1‐q15 microdeletion in a male patient with severe autistic disorder, lack of oral language, and dysmorphic features with concomitant presence of a maternally inherited Xp22.31 copy number gain [PDF]
Clinical Case Reports (discontinued), 2015 We report on a male patient with severe autistic disorder, lack of oral language, and dysmorphic features who carries a rare interstitial microdeletion of 4.96 Mb at chromosome 6q14.1‐q15.
Inés Quintela +2 more
exaly +2 more sources