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Items: 1 to 20 of 118

1.

Development of a rapid multiplex PCR assay for identification of the three common Hemoglobin-Lepore variants (Boston-Washington, Baltimore, and Hollandia) and identification of a new Lepore variant.

Nussenzveig RH, Vanhille DL, Hussey D, Reading NS, Agarwal AM.

Am J Hematol. 2012 Oct;87(10):E74-5. doi: 10.1002/ajh.23304. No abstract available. Erratum in: Am J Hematol. 2012 Dec;87(12):E136. Reading, N Scott [added].

2.

First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA₂-NYU in Iran.

Amirian A, Karimipoor M, Jafarinejad M, Taghavi M, Kordafshari A, Fathi Azar S, Mohammadi MS, Zeinali S.

Arch Iran Med. 2011 Jan;14(1):8-11. doi: 011141/AIM.003.

3.

Sudanese (δβ)0-Thalassemia: Identification and Characterization of a Novel 9.6 kb Deletion.

Waye JS, Eng B, Got T, Hanna M, Hohenadel BA, Nakamura LM, Walker L.

Hemoglobin. 2015;39(5):368-70. doi: 10.3109/03630269.2015.1057736.

PMID:
26154945
4.

Hb Lepore in the Indian population.

Shaji RV, Edison ES, Krishnamoorthy R, Chandy M, Srivastava A.

Hemoglobin. 2003 Feb;27(1):7-14.

PMID:
12603088
5.

Association of Hb S/Hb lepore and delta beta-thalassemia/Hb lepore in Sicilian patients: review of the presence of Hb lepore in Sicily.

Mirabile E, Testa R, Consalvo C, Dickerhoff R, Schilirò G.

Eur J Haematol. 1995 Aug;55(2):126-30.

PMID:
7543057
6.

Interactions of hemoglobin Lepore (deltabeta hybrid hemoglobin) with various hemoglobinopathies: A molecular and hematological characteristics and differential diagnosis.

Chaibunruang A, Srivorakun H, Fucharoen S, Fucharoen G, Sae-ung N, Sanchaisuriya K.

Blood Cells Mol Dis. 2010 Mar 15;44(3):140-5. doi: 10.1016/j.bcmd.2009.11.008.

PMID:
20022270
7.

Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGH.

Blattner A, Brunner-Agten S, Ludin K, Hergersberg M, Herklotz R, Huber AR, Röthlisberger B.

Blood Cells Mol Dis. 2013 Jun;51(1):39-47. doi: 10.1016/j.bcmd.2013.02.002.

PMID:
23491071
8.

[Delta⁰-thalassemia by insertion of 27 base pairs in δ-globin gene with decreased hemoglobin A₂ levels].

González Borrachero ML, de la Fuente-Gonzalo F, González FA, Nieto JM, Villegas A, Ropero P.

Med Clin (Barc). 2015 Apr 8;144(7):312-6. doi: 10.1016/j.medcli.2014.10.021. Spanish.

PMID:
25579773
9.

Polymerase chain reaction-based search for two alpha-globin gene mutations in India.

Bhattacharya G, Sarkar AA, Banerjee D, Chandra S, Das M, Dasgupta UB.

Hemoglobin. 2008;32(5):485-90. doi: 10.1080/03630260802341620.

PMID:
18932074
10.

A novel 506kb deletion causing εγδβ thalassemia.

Rooks H, Clark B, Best S, Rushton P, Oakley M, Thein OS, Cuthbert AC, Britland A, Ruf A, Thein SL.

Blood Cells Mol Dis. 2012 Oct 15-Dec 15;49(3-4):121-7. doi: 10.1016/j.bcmd.2012.05.010.

PMID:
22677107
11.
12.

Genotype-phenotype relationship of the δ-thalassemia and Hb A(2) variants: observation of 52 genotypes.

Lacerra G, Scarano C, Lagona LF, Testa R, Caruso DG, Medulla E, Friscia MG, Mastrullo L, Caldora M, Prezioso R, Gaudiano C, Magnano C, Romeo MA, Musollino G, Di Noce F, Carestia C.

Hemoglobin. 2010;34(5):407-23. doi: 10.3109/03630269.2010.511586.

PMID:
20854114
13.

Hb CS-H disease combined with beta-thalassemia--a case report.

Huang Y, Lin M, Wu JR, Yang LY, Xiang Z.

Blood Cells Mol Dis. 2010 Apr 15;44(4):215-6. doi: 10.1016/j.bcmd.2010.01.003. No abstract available.

PMID:
20116304
14.

Co-inheritance of β- and δ-thalassemia compromising prenatal screening in a Chinese couple seeking prevention.

Li J, Xie XM, Zhou JY, Li DZ.

Fetal Diagn Ther. 2011;30(1):73-6. doi: 10.1159/000321046.

PMID:
21494010
15.

Hemoglobin variants in Cyprus.

Kyrri AR, Felekis X, Kalogerou E, Wild BJ, Kythreotis L, Phylactides M, Kleanthous M.

Hemoglobin. 2009;33(2):81-94. doi: 10.1080/03630260902813502.

PMID:
19373583
16.

β-Thalassemia Intermedia Caused by Compound Heterozygosity for Hb Lepore-Hollandia and β-Thalassemia is Rare in the Indian Population.

Sreedharanunni S, Chhabra S, Hira JK, Bansal D, Sharma P, Das R.

Hemoglobin. 2015;39(5):362-5. doi: 10.3109/03630269.2015.1064004.

PMID:
26291970
17.

Fetal hemoglobin elevation in Hb Lepore heterozygotes and its correlation with beta globin cluster linked determinants.

Gonçalves I, Henriques A, Raimundo A, Picanço I, Reis A, Correia Junior E, Santos E, Nogueira P, Osório-Almeida L.

Am J Hematol. 2002 Feb;69(2):95-102.

PMID:
11835344
18.

Detection of anti-Lepore Hb P-Nilotic by multiplex ligation-dependent probe amplification.

Cui J, Azimi M, Adekile AD, Al Awadhi H, Hoppe CC.

Hemoglobin. 2012;36(3):276-82. doi: 10.3109/03630269.2012.660901.

PMID:
22384950
19.

Detection of Hb anti-Lepore Hong Kong (NG_000007.3: g.63154_70565dup) in Chinese individuals.

Lou JW, He Y, Liu YH, Zhong BM, Zhao Y, He XX, Li DZ.

Hemoglobin. 2014;38(2):146-8. doi: 10.3109/03630269.2013.875477.

PMID:
24471736
20.

Co-inheritance of compound heterozygous Hb Constant Spring and a single -alpha(3.7) gene deletion with heterozygous deltabeta thalassaemia: a diagnostic challenge.

Azma RZ, Othman A, Azman N, Alauddin H, Ithnin A, Yusof N, Razak NF, Sardi NH, Hussin NH.

Malays J Pathol. 2012 Jun;34(1):57-62.

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