(Q44553788)

4 December 2017

Two beta-thalassemia mutations in Japan: codon 121 (GAA----TAA) and IVS-I-130 (G----C). (English)

1 reference

4 December 2017

1 reference

Yamamoto K

1

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4 December 2017

Yamamoto K

2

1 reference

4 December 2017

Hattori Y

3

1 reference

4 December 2017

Yamashiro Y

4

1 reference

4 December 2017

Hoshitani M

5

1 reference

4 December 2017

Morishita M

6

1 reference

4 December 2017

Ohba Y

7

1 reference

4 December 2017

Katahira H

8

1 reference

4 December 2017

Karasawa M

9

1 reference

4 December 2017

Omine M

10

1 reference

4 December 2017

1 January 1992

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4 December 2017

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4 December 2017

16

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4 December 2017

4

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4 December 2017

295-302

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Inclusion-body beta-thalassemia trait. A form of beta thalassemia producing clinical manifestations in simple heterozygotes.

4 December 2017

1 reference

https://api.crossref.org/works/10.3109%2F03630269208998872

Molecular basis for dominantly inherited inclusion body beta-thalassemia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03630269208998872

Beta-thalassemia in Turkey

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03630269208998872

Construction of human gene libraries from small amounts of peripheral blood: analysis of beta-like globin genes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03630269208998872

DNA sequencing with chain-terminating inhibitors

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03630269208998872

Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03630269208998872

A single nucleotide deletion in codon 123 of the beta-globin gene causes an inclusion body beta-thalassaemia trait: a novel elongated globin chain beta Makabe

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03630269208998872

beta-Thalassemia in American Blacks: novel mutations in the "TATA" box and an acceptor splice site

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03630269208998872

The beta zero-thalassemia in an American black family is due to a single nucleotide substitution in the acceptor splice junction of the second intervening sequence

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03630269208998872

A single-base change at a splice site in a beta 0-thalassemic gene causes abnormal RNA splicing.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03630269208998872

Analysis of enzymatically amplified β-globin and HLA-DQα DNA with allele-specific oligonucleotide probes

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F03630269208998872

10.3109/03630269208998872

21 January 2018

Identifiers

DOI

1 reference

4 December 2017

1 reference