نتایج جستجو برای: chromosome abnormalities

تعداد نتایج: 214354  

Journal: :The Journal of Clinical Endocrinology & Metabolism 1996

Journal: :The Ulster Medical Journal 2003
P. McGrattan M. W. Humphreys

M4Eo acute myeloid leukaemia (AML) patients with the typical chromosome 16 abnormalities have a favourable prognosis. These subtle 16q22 gene rearrangements can be difficult to detect by conventional cytogenetic methods and if missed could lead to the incorrect assignment of prognostic group and hence subsequent treatment strategies. We retrospectively studied 13 patients diagnosed with M4Eo AM...

Journal: :Environmental Health Perspectives 1990
T Hashimoto M Ohtaki N Kamada H Yamamoto M Munaka

Relationships among additional chromosome abnormalities in chronic myelocytic leukemia (CML) with translocation 9;22 [Philadelphia chromosome (Ph1)-positive CML] were analyzed by log-linear models on 709 karyotypes reported in the literature. Additional abnormalities, such as the gain of chromosome 8 (+8), gain of Philadelphia chromosome (+Ph1), isochromosome of the long arm (q) of chromosome 1...

2014
Fadlalla Elfateh Ruixue Wang Zhihong Zhang Yuting Jiang Shuang Chen Ruizhi Liu

BACKGROUND Wide range of disorders ranging from genetic disorders to coital difficulties can influence male fertility. In this regard, genetic factors are highlighted as the most frequent, contributed to 10-15%, of male infertility causes. OBJECTIVE To investigate the influence of genetic abnormalities on semen quality and reproductive hormone levels of infertile men from Northeast China. M...

Journal: :Blood 2002
Jaroslaw P Maciejewski Antonio Risitano Elaine M Sloand Olga Nunez Neal S Young

A serious complication of aplastic anemia (AA) is its evolution to clonal hematologic diseases such as myelodysplasia (MDS) and leukemia, which is usually associated with the appearance of a cytogenetic abnormality in bone marrow cells. We present here an analysis of a cohort of 30 patients with otherwise typical AA in whom clonal karyotypic evolution was observed during frequent periodic marro...

Journal: :Genetics and molecular research : GMR 2014
Y Dong L L Li R X Wang X W Yu X Yun R Z Liu

The subsequent reproductive outcomes in couples with a history of recurrent pregnancy loss (RPL) associated with chromosome abnormalities or polymorphisms are generally not reported in China. Many RPL carrier couples have decided not to have children. The present study recorded the subsequent delivery, miscarriage, and unpregnancy outcomes of 113 RPL carrier couples and 226 non-carrier couples,...

Journal: :Genes & genetic systems 2004
Koichiro Tsunewaki

Of the various chlorophyll abnormalities that occur in polyploid wheats, genetic bases of only two types, chlorina and virescence, are known. Here, for the first time, the chromosomal bases of three other chlorophyll abnormalities, striato-virescence, delayed virescence, and albino, which occur in Emmer wheat (2n = 4x = 28, genome constitution AABB) are reported. A set of disomic substitution l...

2011
Simona Baronchelli Donatella Conconi Elena Panzeri Angela Bentivegna Serena Redaelli Sara Lissoni Fabiana Saccheri Nicoletta Villa Francesca Crosti Elena Sala Emanuela Martinoli Marinella Volontè Anna Marozzi Leda Dalprà

The importance of X chromosome in the aetiology of premature ovarian failure (POF) is well-known but in many cases POF still remains idiopathic. Chromosome aneuploidy increase is a physiological phenomenon related to aging, but the role of low-level sex chromosome mosaicism in ovarian function is still undiscovered. Standard cytogenetic analysis was carried out in a total of 269 patients affect...

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