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2017 | 1 |
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Page 1
Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases.
Mol Genet Genomic Med. 2019 Aug;7(8):e820. doi: 10.1002/mgg3.820. Epub 2019 Jun 18.
Mol Genet Genomic Med. 2019.
PMID: 31210028
Free PMC article.
Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient.
Taghdiri M, Kashef A, Abbassi G, Moshtagh A, Sadatian N, Fardaei M, Najafi K, Kariminejad R.
Taghdiri M, et al. Among authors: moshtagh a.
Clin Case Rep. 2019 May 4;7(6):1149-1153. doi: 10.1002/ccr3.2020. eCollection 2019 Jun.
Clin Case Rep. 2019.
PMID: 31183084
Free PMC article.
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Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis.
Najafi K, Kariminejad R, Hosseini K, Moshtagh A, Abbassi GM, Sadatian N, Bazrgar M, Kariminejad A, Kariminejad MH.
Najafi K, et al. Among authors: moshtagh a.
Case Rep Genet. 2017;2017:2706098. doi: 10.1155/2017/2706098. Epub 2017 Jan 4.
Case Rep Genet. 2017.
PMID: 28133555
Free PMC article.
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Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18.
Kariminejad A, Kariminejad R, Moshtagh A, Zanganeh M, Kariminejad MH, Neuenschwander S, Okoniewski M, Wey E, Schinzel A, Baumer A.
Kariminejad A, et al. Among authors: moshtagh a.
Eur J Hum Genet. 2011 May;19(5):555-60. doi: 10.1038/ejhg.2010.252. Epub 2011 Feb 16.
Eur J Hum Genet. 2011.
PMID: 21326286
Free PMC article.
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