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Identification of Chromosome Abnormalities in Subtelomeric Regions Using Multiplex Ligation Dependent Probe Amplification (MLPA) Technique in 100 Iranian Patients With Idiopathic Mental Retardation.
Iran Red Crescent Med J. 2013 Oct;15(10):e8221. doi: 10.5812/ircmj.8221. Epub 2013 Oct 5.
Iran Red Crescent Med J. 2013.
PMID: 24693374
Free PMC article.
Fraccaro syndrome: report of two Iranian cases: an infant and an adult in a family.
Hadipour F, Shafeghati Y, Bagherizadeh E, Behjati F, Hadipour Z.
Hadipour F, et al. Among authors: bagherizadeh e.
Acta Med Iran. 2013;51(12):907-9.
Acta Med Iran. 2013.
PMID: 24442548
Free article.
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Phenotypical characterization of 13q deletion syndrome: Report of two cases.
Bagherizadeh E, Shafaghati Y, Hadipour F, Behjati F.
Bagherizadeh E, et al.
Indian J Hum Genet. 2014 Apr;20(2):203-5. doi: 10.4103/0971-6866.142912.
Indian J Hum Genet. 2014.
PMID: 25400354
Free PMC article.
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Prenatal diagnosis in a mentally retarded woman with mosaic ring chromosome 18.
Bagherizadeh E, Behjati F, Saberi SH, Shafeghati Y.
Bagherizadeh E, et al.
Indian J Hum Genet. 2011 May;17(2):111-3. doi: 10.4103/0971-6866.86201.
Indian J Hum Genet. 2011.
PMID: 22090726
Free PMC article.
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Triploidy in a fetus following amniocentesis referred for maternal serum screening test at second trimester.
Bagherizadeh E, Oveisi M, Hadipour Z, Saremi A, Shafaghati Y, Behjati F.
Bagherizadeh E, et al.
Indian J Hum Genet. 2010 May;16(2):94-6. doi: 10.4103/0971-6866.69371.
Indian J Hum Genet. 2010.
PMID: 21031058
Free PMC article.
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