نتایج جستجو برای: cytogenetic study

تعداد نتایج: 3977050  

Journal: :European Psychiatry 2023

Introduction Turner syndrome characterized by total/partial and/or homogeneous/mosaic X chromosome monosomy is associated with various physical health concerns, including facial dysmorphism, short stature, infertility, and other organ defects such as heart, kidney, bone, skin, … well variable degrees of cognitive impairments. Besides, social skills, communication relationships are usually disor...

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...

2000
Hagop M. Kantarjian

We read with interest the report of Hehlmann et all in which 133 patients were randomized to interferon-a (IFN-a) therapy (5 X lo6 U/m2/d). The incidence of complete hematologic response. (CHR) was 31% and of complete cytogenetic response was 7%. Their median survival was 5.5 years, which was superior to that of 186 patients treated with busulfan (median survival, 3.8 years; P = .008), but simi...

Journal: :Blood 1995
H M Kantarjian M Talpaz

We read with interest the report of Hehlmann et all in which 133 patients were randomized to interferon-a (IFN-a) therapy (5 X lo6 U/m2/d). The incidence of complete hematologic response. (CHR) was 31% and of complete cytogenetic response was 7%. Their median survival was 5.5 years, which was superior to that of 186 patients treated with busulfan (median survival, 3.8 years; P = .008), but simi...

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...

Journal: :World journal of pediatrics : WJP 2015
Sharmila Thillainathan Nirmala D Sirisena Kariyawasam W J C Kariyawasam Rohan W Jayasekara Vajira H W Dissanayake

BACKGROUND Cytogenetic analysis is a valuable investigation in the diagnostic work up of children with suspected chromosomal disorders. The objective of this study was to describe the prevalence of various types of chromosomal abnormalities in Sri Lankan children undergoing cytogenetic analysis. METHODS Cytogenetic reports of 1554 consecutive children with suspected chromosomal disorders who ...

Journal: :Occupational and Environmental Medicine 1991

Journal: :cell journal 0

objective: chromosomal aberrations are common causes of multiple anomaly syndromes. recurrent chromosomal aberrations have been identified by conventional cytogenetic methods used widely as one of the most important clinical diagnostic techniques. materials and methods: in this retrospective study, the incidences of chromosomal aberrations were evaluated in a six year period from 2005 to 2011 i...

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