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Items: 5

1.

Evaluation of point mutations in dystrophin gene in Iranian Duchenne and Becker muscular dystrophy patients: introducing three novel variants.

Haghshenas M, Akbari MT, Karizi SZ, Deilamani FK, Nafissi S, Salehi Z.

J Genet. 2016 Jun;95(2):325-9.

2.

Population data of 13 nonCODIS STR markers located inside the 6 nonsyndromic oculocutaneous albinism genes.

Khordadpoor Deilamani F, Akbari MT.

Int J Legal Med. 2016 Nov;130(6):1485-1486. Epub 2016 Mar 1.

PMID:
26932870
3.

Homozygosity mapping in albinism patients using a novel panel of 13 STR markers inside the nonsyndromic OCA genes: introducing 5 novel mutations.

Khordadpoor-Deilamani F, Akbari MT, Karimipoor M, Javadi GR.

J Hum Genet. 2016 May;61(5):373-9. doi: 10.1038/jhg.2015.167. Epub 2016 Jan 28.

PMID:
26818737
4.

Sequence analysis of tyrosinase gene in ocular and oculocutaneous albinism patients: introducing three novel mutations.

Khordadpoor-Deilamani F, Akbari MT, Karimipoor M, Javadi G.

Mol Vis. 2015 Jul 10;21:730-5. eCollection 2015.

5.

Dystrophin gene mutation analysis in Iranian males and females using multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification methods.

Khordadpoor-Deilamani F, Akbari MT, Nafissi S, Zamani G.

Genet Test Mol Biomarkers. 2011 Dec;15(12):893-9. doi: 10.1089/gtmb.2011.0057. Epub 2011 Aug 4.

PMID:
21815800

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