نتایج جستجو برای: Chromosome 9

تعداد نتایج: 593632  

Journal: :iranian journal of public health 0
m khaleghian c azimi

pericentric inversions of chromosome 9 are among the most frequent chromosomal rearrangement in human. a few cytogeneticists consider inversions of chromosome 9 as a normal variant. however, many reports in the recent literature link pericentric inversions of chromosome 9 with infertility, recurrent abortions, and a number of other abnormal conditions. we report a case of homozygosity pericentr...

Journal: :Gulustan-Black Sea Scientific Journal of Academic Research 2019

F. Ashrafzadeh, M. Faraji

Oculo-auriculovertebral dysplasia (Goldenhar) is a congenital syndrome. Its phenotype differs from craniofacial anomalies to cardiac, vertebral or central nervous system defects. This syndrome is rare and its etiology is not apparent yet. Pericentric inversion of chromosome 9 is one of the most common structural balanced chromosomal aberrations with its incidences 15% to 25%. Herein we present ...

Journal: :Molecular Cytogenetics 2013

Journal: :iranian journal of medical sciences 0
f. ashrafzadeh m. faraji

oculo-auriculovertebral dysplasia (goldenhar) is a congenital syndrome. its phenotype differs from craniofacial anomalies to cardiac, vertebral or central nervous system defects. this syndrome is rare and its etiology is not apparent yet. pericentric inversion of chromosome 9 is one of the most common structural balanced chromosomal aberrations with its incidences 15% to 25%. herein we present ...

Journal: :international journal of reproductive biomedicine 0
fatemeh baghbani salmeh mirzaee mohammad hassanzadeh-nazarabadi

background: chromosomal disorders are the most common cause of first trimester spontaneous abortion. among the human chromosomes, chromosome no.9 was the most common structural chromosomal variant and it is not thought to be of any functional importance, which often considers as a normal variation in structural polymorphisms, nevertheless there are some studies which claim that there is an asso...

Journal: :Journal of Medical Genetics 1971

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