Results 221 to 230 of about 55,105 (243)
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Sotos syndrome with a balanced reciprocal translocation t(2;12)(q33.3;q15).

Annales de genetique, 1990
A balanced reciprocal translocation, 46,XY, t(2;12), was detected in a male infant who had the characteristic features of Sotos syndrome. His father's karyotype was normal, but his mother and an older brother had the same chromosomal abnormality without a history or clinical features of Sotos syndrome.
K, Tamaki   +6 more
openaire   +1 more source

Adsorption Mechanism and Inhibition Efficiency of Quaternium-15 (Q15) Surfactant on Carbon Steel in 1 M HCl: A Combined Theoretical and Experimental Approach

Results in Engineering
M. Afifi   +7 more
semanticscholar   +1 more source

Gesundheitskompetenz im Kindesalter messen mit dem HLS-Child-Q15

2022
Bollweg, Torsten Michael   +6 more
openaire   +1 more source

A novel t(6;13)(q15;q34) translocation in a giant cell reparative granuloma (solid aneurysmal bone cyst).

Human Pathology, 2012
Zenggang Pan   +5 more
semanticscholar   +1 more source

A BACH2‐BCL2L1 fusion gene resulting from a t(6;20)(q15;q11.2) chromosomal translocation in the lymphoma cell line BLUE‐1

Genes, Chromosomes and Cancer, 2011
S. Türkmen   +5 more
semanticscholar   +1 more source

Translocation (1;4;12)(q25;q27;q15) in a childhood intramuscular lipoma

Cancer Genetics and Cytogenetics, 2005
Liming Bao, Lili Miles
openaire   +1 more source

The t(1;9)(p34;q34) and t(8;12)(p11;q15) fuse pre‐mRNA processing proteins SFPQ (PSF) and CPSF6 to ABL and FGFR1

Genes, Chromosomes and Cancer, 2008
Claire E Hidalgo-Curtis   +8 more
semanticscholar   +1 more source

ASK1 (MAP3K5) as a potential therapeutic target in malignant fibrous histiocytomas with 12q14–q15 and 6q23 amplifications

Genes, Chromosomes and Cancer, 2004
F. Chibon   +8 more
semanticscholar   +1 more source

Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32→q33 and 12q14→q15

Cytogenetic and Genome Research, 2005
M. Nilsson   +4 more
semanticscholar   +1 more source

DFNB74, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 12q14.2‐q15

Clinical Genetics, 2009
A. Waryah   +8 more
semanticscholar   +1 more source

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