Results 191 to 200 of about 10,505 (217)
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A New and Unusual Reciprocal Translocation in Cattle: rcp(11;25)(q11;q14–21)
Cytogenetic and Genome Research, 2011A new and unusual reciprocal translocation was detected in a heifer of the Agerolese cattle breed during a routine cytogenetic screening carried out on 13 animals (2 males and 11 females) kept at the ConSDABI Conservation Center in Benevento (Southern Italy).
A. Perucatti +9 more
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A case of alveolar rhabdomyosarcoma with a chromosomal translocation, t(2; 13) (q37; q14)
Virchows Archiv A Pathological Anatomy and Histopathology, 1990We report on an alveolar rhabdomyosarcoma occurring in a 17-year-old girl. Histologically, the tumour exhibited a proliferation of small, round cells and formed alveolar structures. Immunohistochemical studies of the tumour cells showed desmin and creatine kinase MM positivity.
T, Nojima +4 more
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MDM2 amplification in a primary alveolar rhabdomyosarcoma displaying a t(2;13)(q35;q14)
Cytogenetics and Cell Genetics, 2008This report describes a case of rhabdomyosarcoma associated with a 2;13 translocation and multiple double minute chromosomes. The origin of the amplified DNA was identified using comparative genomic hybridization, which pinpointed a unique spot at 12q→13q14.
M, Meddeb +8 more
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Localization of the gene for human erythrocyte glycophorin C to chromosome 2, q14–q21
Human Genetics, 1986A complementary cDNA clone (900 bp) representing the 3' untranslated region and almost the entire coding sequence of the human erythrocyte membrane glycophorin C has been used to determine the chromosomal location of the blood group Gerbich locus by in situ hybridization.
M G, Mattei +4 more
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The Journal of Pediatrics, 1982
Hypereosinophilic syndrome is probably a disease of diverse etiologies. We studied the bone marrow of a patient with HES and found a population of L-1 lymphoblasts. These cells failed to grow in double-layer agar cultures, were "null cells," and contained a 14q+ marker chromosome consistent with a malignant lymphoproliferative disorder.
R R, Chilcote +3 more
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Hypereosinophilic syndrome is probably a disease of diverse etiologies. We studied the bone marrow of a patient with HES and found a population of L-1 lymphoblasts. These cells failed to grow in double-layer agar cultures, were "null cells," and contained a 14q+ marker chromosome consistent with a malignant lymphoproliferative disorder.
R R, Chilcote +3 more
openaire +2 more sources
Duplication of 15q11.2-q14, including theP gene, in a woman with generalized skin hyperpigmentation
American Journal of Medical Genetics, 2001We describe a woman with 15q11.2-q14 duplication who had clinical manifestations of proximal 15q trisomy and hyperpigmentation. Within this region, the P gene, located at chromosome segment 15q11.2-q12, is associated with oculocutaneous albinism type II (OCA2) and with hypopigmentation in the Prader-Willi and Angelman chromosome 15q deletion syndromes.
K, Akahoshi +5 more
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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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Translocation (2;13)(q37;q14) in rhabdomyosarcoma: A new case
Cancer Genetics and Cytogenetics, 1987J L, Lai +4 more
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Querschnittsfach Schmerzmedizin Q14 – das Mainzer Modell
Der Schmerz, 2017S. Kurz +3 more
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