Genetic basis of persistent red blood cell microcytosis in the Chinese unexplained by phenotypical testing.

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Genetic basis of persistent red blood cell microcytosis in the Chinese unexplained by phenotypical testing.

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2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年學術文章

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2014年學術文章

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Genetic basis of persistent re ...... ained by phenotypical testing.

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Genetic basis of persistent re ...... ained by phenotypical testing.

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Genetic basis of persistent re ...... ained by phenotypical testing.

@en

Genetic basis of persistent re ...... ained by phenotypical testing.

@nl

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Genetic basis of persistent re ...... ained by phenotypical testing.

@en

Genetic basis of persistent re ...... ained by phenotypical testing.

@nl

P1476

Genetic basis of persistent re ...... ained by phenotypical testing.

@en

P2093

Ada K Liu

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Amy Y Chan

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Chi-Chiu So

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Donna Y Ngai

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Kin-Sang Leung

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Mandy H Tsang

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P2860

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A laboratory strategy for genotyping haemoglobin H disease in the Chinese.

Detection and characterisation of beta-globin gene cluster deletions in Chinese using multiplex ligation-dependent probe amplification.

Simple method for screening of alpha-thalassaemia 1 carriers.

Hematological characteristics and effective screening for compound heterozygosity for Hb constant spring and deletional α+ -thalassemia.

A multicenter trial of the effectiveness of zeta-globin enzyme-linked immunosorbent assay and hemoglobin H inclusion body screening for the detection of alpha0-thalassemia trait.

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69-72

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P31

scholarly article

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10.1136/JCLINPATH-2014-202568

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English

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P478

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P577

2014-10-28T00:00:00Z

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P698

25352644

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