Hamid M - Search Results

1

Exon sequencing of PKD1 gene in an Iranian patient with autosomal-dominant polycystic kidney disease.

Hafizi A, Khatami SR, Galehdari H, Shariati G, Saberi AH, Hamid M. Hafizi A, et al. Among authors: hamid m. Iran Biomed J. 2014 Jul;18(3):143-50. doi: 10.6091/ibj.1317.2014. Iran Biomed J. 2014. PMID: 24842140 Free PMC article.

2

Transient expression assay of Agamma-588 (A/G) mutations in the K562 cell line.

Hamid M, Mahjoubi F, Akbari MT, Khanahmad H, Jamshidi F, Zeinali S, Karimipoor M. Hamid M, et al. Iran Biomed J. 2011;15(1-2):15-21. Iran Biomed J. 2011. PMID: 21725495 Free PMC article.

3

Identification of α-globin chain variants: a report from Iran.

Akbari MT, Hamid M. Akbari MT, et al. Among authors: hamid m. Arch Iran Med. 2012 Sep;15(9):564-7. Arch Iran Med. 2012. PMID: 22924376

4

Hb AHVAZ [α83(F4)Leu→Arg, CTG>CGG (α2); HBA2: c.251T>G],a new hemoglobin variant of the α2-globin gene.

Hamid M, Shariati G, Saberi A, Galehdari H, Kaikhaei B, Mohammadi-Anaei M. Hamid M, et al. Hemoglobin. 2013;37(5):477-80. doi: 10.3109/03630269.2013.792095. Epub 2013 May 15. Hemoglobin. 2013. PMID: 23672273

5

Identification of IVS-I (-1) (G > C) or Hb Monroe as a report on the beta-globin gene with a beta-thalassemia minor phenotype in south of Iran.

Hamid M, Shariati G, Saberi A, Kaikhaei B, Galehdari H, Mohammadi-Anaei M. Hamid M, et al. Arch Iran Med. 2013 Sep;16(9):563-4. Arch Iran Med. 2013. PMID: 23981164

6

A novel alpha-thalassemia nonsense mutation in HBA2: C.382 A > T globin gene.

Hamid M, Bokharaei Merci H, Galehdari H, Saberi AH, Kaikhaei B, Mohammadi-Anaei M, Ahmadzadeh A, Shariati G. Hamid M, et al. Arch Iran Med. 2014 Jul;17(7):475-6. Arch Iran Med. 2014. PMID: 24979558

7

Wolf-Hirschhorn syndrome: a case with normal karyotype, demonstrated by array CGH (aCGH).

Saberi A, Shariati G, Hamid M, Galehdari H, Abdorasouli N. Saberi A, et al. Among authors: hamid m. Arch Iran Med. 2014 Sep;17(9):642-4. Arch Iran Med. 2014. PMID: 25204484

8

Molecular prenatal diagnosis of megalencephalic leukoencephalopathy with subcortical cysts in a child from southwest of Iran.

Shariati G, Hamid M, Saberi A, Andashti B, Galehdari H. Shariati G, et al. Among authors: hamid m. Clin Case Rep. 2015 Feb;3(2):114-7. doi: 10.1002/ccr3.168. Epub 2014 Nov 26. Clin Case Rep. 2015. PMID: 25767710 Free PMC article.

9

The First Report of a 290-bp Deletion in β-Globin Gene in the South of Iran.

Hamid M, Dawoody Nejad L, Shariati G, Galehdari H, Saberi A, Mohammadi-Anaei M. Hamid M, et al. Iran Biomed J. 2017 Mar;21(2):126-8. doi: 10.18869/acadpub.ibj.21.2.126. Epub 2016 Mar 8. Iran Biomed J. 2017. PMID: 26948378 Free PMC article.

10

Mutation Screening of the Krüppel-like Factor 1 Gene in Individuals With Increased Fetal Hemoglobin Referred for Hemoglobinopathy Investigation in South of Iran.

Hamid M, Ershadi Oskouei S, Shariati G, Babaei E, Galehdari H, Saberi A, Sedaghat A. Hamid M, et al. J Pediatr Hematol Oncol. 2018 Apr;40(3):192-195. doi: 10.1097/MPH.0000000000001093. J Pediatr Hematol Oncol. 2018. PMID: 29420372

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