نتایج جستجو برای: clasical cytogenetics

تعداد نتایج: 10228  

2017
Marion Imbert-Bouteille Jean Chiesa Jean-Baptiste Gaillard Véronique Dorvaux Lucille Altounian Vincent Gatinois Eve Mousty Sanae Finge Pascal Bourquard Joris Robert Vermeesch Eric Legius Peter Vandenberghe

Medical Genetics and Cytogenetics Department, Carémeau University Hospital Center, Nîmes, France Medical Genetics and Cytogenetics Department, University Hospital Center, Montpellier, France Hematology Department, Mercy Hospital Center of Metz‐Thionville, Metz, France Cytogenetics Department, Mercy Hospital Center of Metz‐Thionville, Metz, France Multidisciplinary Prenatal Diagnosis Department,...

Journal: :Blood 2010
Miriam Miesner Claudia Haferlach Ulrike Bacher Tamara Weiss Katja Macijewski Alexander Kohlmann Hans-Ulrich Klein Martin Dugas Wolfgang Kern Susanne Schnittger Torsten Haferlach

The World Health Organization classification of acute myeloid leukemia (AML) is hierarchically structured and integrates genetics, data on patients' history, and multilineage dysplasia (MLD). The category "AML with myelodysplastic syndrome (MDS)-related changes" (AML-MRC) is separated from "AML not otherwise specified" (AML-NOS) by presence of MLD, MDS-related cytogenetics, or history of MDS or...

2017
Po‐Han Lin Huei‐Ying Li Sheng‐Chih Fan Tzu‐Hang Yuan Ming Chen Yu‐Hua Hsu Yu‐Hsuan Yang Long‐Yuan Li Su‐Peng Yeh Li‐Yuan Bai Yu‐Min Liao Chen‐Yuan Lin Ching‐Yun Hsieh Ching‐Chan Lin Che‐Hung Lin Ming‐Yu Lien Tzu‐Ting Chen Yen‐Hsuan Ni Chang‐Fang Chiu

Conventional cytogenetics can categorize patients with acute myeloid leukemia (AML) into favorable, intermediate, and unfavorable-risk groups; however, patients with intermediate-risk cytogenetics represent the major population with variable outcomes. Because molecular profiling can assist with AML prognosis and next-generation sequencing allows simultaneous sequencing of many target genes, we ...

2017
Jing SHA Fumin LIU Bei ZHANG Yang HUANG Qinglin ZHANG Gao JUAN Jingfang ZHAI

Trisomy 13 (Patau syndrome) is the third most common autosomal trisomy with a prevalence between 1 in 10,000 - 20,000 live births. Robertsonian translocations represent the largest number of chromosomal aberrations in human population with an incidence of 1.23 in 1000 live birth and translocation 13;14 is one of the most frequent Robertsonian translocations (approximately 75%). We sampled umbil...

Journal: :Haematologica 2001
N B Westwood A M Gruszka-Westwood S Atkinson T C Pearson

BACKGROUND AND OBJECTIVES The diagnosis of polycythemia vera (PV) is supported by the finding of an abnormal karyotype in patients with erythrocytosis. However, most PV patients have normal marrow cytogenetics at presentation and there is reluctance to use this test routinely. Comparative genomic hybridization (CGH) is a cytogenetic screening technique that analyzes interphase cells. This appro...

Journal: :Cytogenetic and genome research 2008
M Breen

Humans and dogs have coexisted for thousands of years, during which time we have developed a unique bond, centered on companionship. Along the way, we have developed purebred dog breeds in a manner that has resulted unfortunately in many of them being affected by serious genetic disorders, including cancers. With serendipity and irony the unique genetic architecture of the 21st century genome o...

Journal: :School Education Journal PGSD FIP Unimed 2021

This purposes of this research is to improve learning result on science subject through google classroom application. Google can be used assist students in developing problem solving skills action conducted by 2 cycles the four phases: planning, implementation, observation, reflection. The subjects were from class VII- Junior High School State Tebing Tinggi which amounted 37 students. study a q...

Journal: :Human Reproduction 1996

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

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