نتایج جستجو برای: tetrasomy

تعداد نتایج: 240  

Journal: :Journal of Medical Genetics 1994

Journal: :Zhongguo shi yan xue ye xue za zhi 2004
Hui-Ping Wang Guo-Xia Li Zhen-Hua Qiao Wen-Ying Ren Hong-Wei Wang

This study was purposed to characterize the first case of acute promyelocitic leukemia (AML-M(3a)) with t(15;17), trisomy 8 and tetrasomy 8, and explore its characteristics of morphology, cytogenetics, molecular biology, immunology and clinical features. Morphological changes of peripheral blood and bone marrow smears were observed under microscope. Chromosome specimen was prepared by 24 h shor...

Journal: :Haematologica 2004
Robert Escher Dominique Mühlematter Hamish S Scott Martine Jotterand Andreas Tobler

Atypical chronic myeloid leukemia (aCML) is a rare leukemic disorder with no specific genetic lesion. Here we demonstrate clonal occurrences of tetrasomy for the long arm of chromosome 21 in a patient with aCML, and a thorough review of the literature provides evidence that this chromosomal anomaly is a so far not recognised recurrent finding in aCML. Further, the timely association of the occu...

Journal: :Journal of Medical Genetics 1983

Journal: :Atlas of Genetics and Cytogenetics in Oncology and Haematology 2011

Journal: :Journal of medical genetics 1994
W P Robinson F Binkert A A Schinzel S Basaran R Mikelsaar

Journal: :Cancer research 1997
S A Southern M F Evans C S Herrington

We have analyzed 60 low-grade cervical squamous intraepithelial lesions for low- and high-risk human papillomaviruses (HPVs) and for numerical abnormalities of chromosomes 1, 3, 11, 17, and 18 and the X chromosome. Eleven of 33 lesions infected with high-risk HPVs (HPV 16, 18, 30, 31, 33, 35, 39, 45, 51, 52, 56, 58, and 66) but none of 24 lesions infected with low-risk HPVs (HPV 6, 11, 42, 43, ...

Journal: :American journal of medical genetics. Part A 2012
Kosuke Izumi Laura K Conlin Donna Berrodin Christopher Fincher Alisha Wilkens Chad Haldeman-Englert Sulagna C Saitta Elaine H Zackai Nancy B Spinner Ian D Krantz

Pallister-Killian syndrome (PKS) is a multisystem sporadic genetic condition characterized by facial anomalies, variable developmental delay and intellectual impairment, hypotonia, hearing loss, seizures, pigmentary skin differences, temporal alopecia, diaphragmatic hernia, congenital heart defects, and other systemic abnormalities. PKS is typically caused by the presence of a supernumerary iso...

Journal: :Carcinogenesis 2006
Andrew J Olaharski Rita Sotelo Gilberto Solorza-Luna Maria E Gonsebatt Patricia Guzman Alejandro Mohar David A Eastmond

Chromosomal instability as manifested by increases in aneuploidy and structural chromosome aberrations is believed to play a critical role in the intermediate to late stages in the development of cervical malignancies. The current study was designed to determine the role of tetraploidy in the formation of aneuploidy and ascertain the occurrence of these alterations during the earlier stages of ...

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