نتایج جستجو برای: chromosomal abnormality

تعداد نتایج: 189386  

M GHorbanianfard M.H Daei-Parizi M.H Karininejhad

monosomy 21 is a rare chromosomal abnormality which is persented in mosaic or homogenous forms.the latter form which is very rare,is determined by intra uterin growth retardation)IUGR),failure to thrive (FTT),prominent craniofacial,skeletal deformities and differnt degrees of delay in psychomotor activities.we report an eight years old boy who was admitted in pediatric ward(hospital No 1 of Ker...

Journal: :Blood 1988
H Hirai M Okada H Mizoguchi H Mano Y Kobayashi J Nishida F Takaku

The relationship between chromosomal abnormality and oncogene activation was investigated during leukemic progression in two patients with myelodysplastic syndrome (MDS). Both patients had partial or complete deletion of chromosome 5 in metaphase cells obtained throughout the progression to leukemia. Analysis with specific oligonucleotide probes revealed that bone marrow cells containing an act...

حوری سپهری, , زهرا اوسطی آشتیانی, , فرخنده بهجتی, , محمدتقی اکبری, , پریسا کلانتری, ,

In this study, chromosome analyses were performed on 70 infertile Azoospermic and Oligospermic (<20 million/ml) men, and also cultures of peripheral blood lymphocytes by high resolution banding method were analysed as well. It is revealed 8 (11.43 percent) men with chromosomal abnormality. There were 31.4 percent patients with azoospermia and 68.6 percent with oligospermia from several thousand...

ترکی, یوسف, زمانی, رقیه,

Objective and Background: The incidence of prenatal mortality is one of the most important health indicators of a community. Through identifying factors which bring about prenatal mortality and through raising awareness of pregnant mothers concerning attention to medical cares over pregnancy period, such prenatal mortalities can be remarkably reduced. The main objective of this study was to det...

Journal: :Archives of Iranian medicine 2012
Akbar Safai Mohammad Vasei Armin Attaranzadeh Fariborz Azad Narjes Tabibi

BACKGROUND Secondary amenorrhea is a condition in which there is cessation of menses after at least one menstruation. It is a symptom of different diseases, such as hormonal disturbances which range from pituitary to ovarian origin, as well as chromosomal abnormalities. Knowledge of the distinct cause of secondary amenorrhea is of tremendous benefit for the management and monitoring of patients...

Journal: :Nippon Ronen Igakkai Zasshi. Japanese Journal of Geriatrics 2006

Journal: :Donald School Journal of Ultrasound in Obstetrics and Gynecology 2010

Journal: :international journal of reproductive biomedicine 0
atefeh asgari safieh ghahremani solmaz saeedi ebrahim kamrani

background: different studies show that chromosomal balance translocation in the parents can cause recurrent spontaneous abortions. incidence of chromosomal translocation abnormalities in couples with repeated abortions is from 0% to 31%. objective: the purpose of this research was studying the presence or absence of chromosomal abnormalities and heteromorphism in couples with recurrent abortio...

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