Xmn1-158 γGVariant in B-Thalassemia Intermediate Patients in South-East of Iran.

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Xmn1-158 γGVariant in B-Thalassemia Intermediate Patients in South-East of Iran.

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2017 nî lūn-bûn

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2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

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2017年論文

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2017年论文

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2017年论文

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2017年论文

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Xmn1-158 γGVariant in B-Thalassemia Intermediate Patients in South-East of Iran.

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label

Xmn1-158 γGVariant in B-Thalassemia Intermediate Patients in South-East of Iran.

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prefLabel

Xmn1-158 γGVariant in B-Thalassemia Intermediate Patients in South-East of Iran.

@en

P1476

Xmn1-158 γGVariant in B-Thalassemia Intermediate Patients in South-East of Iran.

@en

P2093

Ali Bazi

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Ebrahim Miri-Moghaddam

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Majid Naderi

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Morteza Karimipoor

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Sara Bahrami

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P2860

Beta-thalassemia

Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia

Amelioration of Sardinian beta0 thalassemia by genetic modifiers.

Thalassaemia intermedia: an update.

Genotyping of BCL11A and HBS1L-MYB SNPs associated with fetal haemoglobin levels: a SNaPshot minisequencing approach

Role of XmnIgG Polymorphism in Hydroxyurea Treatment and Fetal Hemoglobin Level at Isfahanian Intermediate β-Thalassemia Patients.

Regulation of human fetal hemoglobin: new players, new complexities.

Causes of new cases of major thalassemia in sistan and balouchistan province in South-East of iran.

Control of fetal hemoglobin: new insights emerging from genomics and clinical implications.

Beta-thalassemia.

P304

165-171

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P31

scholarly article

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2017-04-01T00:00:00Z

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P698

28875012

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P932

5575729

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