نتایج جستجو برای: cytogenetic abnormalities

تعداد نتایج: 112411  

Journal: :Acta medica portuguesa 2014
Raquel Bastos Carla Ramalho Sofia Dória

INTRODUCTION Spontaneous abortion is one of the most frequent problems of pregnancy, estimated to affect, at least, one in every four women who tries to conceive. The main purpose of this work was to study the prevalence of chromosomal abnormalities in gestational losses, evaluating their relation with maternal age, gestational age and previous abortion history. MATERIAL AND METHODS Retrospec...

2017
Farhad Shahi Razieh Alishahi Hossein Pashaiefar Isa Jahanzad Naser Kamalian Ardeshir Ghavamzadeh Marjan Yaghmaie

Background & Objective Soft tissue sarcomas (STS) constitute an uncommon and heterogeneous group of tumors of mesenchymal origin and various cytogenetic abnormalities ranging from distinct genomic rearrangements, such as chromosomal translocations and amplifications, to more intricate rearrangements involving multiple chromosomes. Fluorescence in situ hybridization (FISH) can be used to identif...

Journal: :cell journal 0

introduction: the incidence of chromosomal abnormalities was investigated in untransfered embryos reuslted from in vitro fertilization (ivf) or intracytoplasmic sperm injection (icsi) procedures. materials and methods: a total of 238 embryos of varying morphology between the pronucleated stage and 8-cells were analysed. the cytogenetic method of dyban was used for chromosome preparation. embryo...

Journal: :Blood 2005
Marco Mancini Daniela Scappaticci Giuseppe Cimino Mauro Nanni Valentina Derme Loredana Elia Agostino Tafuri Marco Vignetti Antonella Vitale Antonio Cuneo Gianluigi Castoldi Giuseppe Saglio Fabrizio Pane Cristina Mecucci Andrea Camera Giorgina Specchia Alessandra Tedeschi Francesco Di Raimondo Giuseppe Fioritoni Francesco Fabbiano Filippo Marmont Felicetto Ferrara Nicola Cascavilla Giuseppe Todeschini Francesco Nobile Maria Grazia Kropp Pietro Leoni Antonio Tabilio Mario Luppi Luciana Annino Franco Mandelli Robin Foà

The Gruppo Italiano Malattie Ematologiche dell'Adulto (GIMEMA) 0496 protocol, through the central handling of bone marrow samples at presentation, allowed us to combine cytogenetic and molecular information on a large series of adults with acute lymphoblastic leukemia (ALL) treated homogeneously, enabling us to define as broadly as possible their genetic profile and to determine the impact on o...

Journal: :Haematologica 2000
N C Gutiérrez J M Hernández J L García J Almeida G Mateo M I González J Hernández J Fernández-Calvo J F San Miguel

BACKGROUND AND OBJECTIVES Cytogenetic studies in multiple myleoma (MM) are limited by the difficulties in obtaining metaphases that can be investigated and few studies have analyzed the relationship between cytogenetics and clinical disease characteristics. The aim of our study was to analyze the recurrent cytogenetic changes in MM and to correlate them with clinical and biological characterist...

Hamid Gourabi Iman Salahshourifar, Mohammad Ali Sadighi Gilani, Najmeh sadat Masoudi

Background The present study offers our contribution on the topic by a retrospective analysis of the prevalence of chromosomal abnormalities in a population of Iranian infertile men attending assisted reproduction programs. MaterialsAndMethods Cytogenetic analysis was performed according to standard methods on cultured cells obtained from the patient peripheral blood. In all, 874 files belongin...

Journal: :Blood 1982
I Shah K Mayeda F Koppitch S Mahmood B Nemitz

Acute myelofibrosis (AMF) was diagnosed in a 59-yr-old black male in September 1978, on the basis of pancytopenia, lack of hepatosplenomegaly, fibrosis of the marrow, and paucity of teardrop red blood cells in the peripheral blood. Since then the patient has demonstrated an unusually long survival of 36 mo with a changing cytogenetic course. His initial 46, XY normal karyotype changed in 20 mo ...

2010
Byung-Sik Cho Hee-Je Kim Ki-Sung Eom Jong-Wook Lee Woo-Sung Min Chun-Choo Kim

Secondary leukemia occurring after hematopoietic stem cell transplantation (HSCT) for acute myeloid leukemia (AML) is rare. Secondary AML usually follows autologous and not allogeneic transplants. When a new leukemia develops in a patient successfully treated with an allogeneic HSCT, the possibility of a de novo or secondary leukemia from either the donor or recipient should be considered. We p...

Journal: :Clinical genetics 2009
S A Yatsenko M C Kruer P I Bader D Corzo J Schuette C E Keegan B Nowakowska S Peacock W W Cai D A Peiffer K L Gunderson Z Ou A C Chinault S W Cheung

Array comparative genomic hybridization studies were performed to further characterize cytogenetic abnormalities found originally by karyotype and fluorescence in situ hybridization in five clinical cases of distal 10q deletions, including several with complex cytogenetic rearrangements and one with a partial male-to-female sex-reversal phenotype. These results have enabled us to narrow the pre...

Journal: :journal of cell and molecular research 0
massoud ranjbar maryam almasi elnaz hosseini

chromosome number, meiotic behavior, and pollen viability were analyzed in 2 species of genus solenanthus, s. stamineus (desf.) wettst. and s. circinnatus ledeb, from iran. this report is the first cytogenetic analysis of these species. all taxa are diploid and possess 2n = 2x = 24 chromosome number, consistent with the proposed base number of x = 12. although this taxon displayed regular bival...

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