(Q44543098)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12908799%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Hb Bronte or alpha93(FG5)Val-->Gly: a new unstable variant of the alpha2-globin gene, associated with a mild alpha(+)-thalassemia phenotype (English)

1 reference

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6 November 2019

3

1 reference

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6 November 2019

author name string

Giuseppina Lacerra

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12908799%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Rosario Testa

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12908799%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Gino Schilirò

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12908799%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

Clementina Carestia

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12908799%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

publication date

1 August 2003

1 reference

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6 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12908799%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

volume

27

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12908799%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12908799%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

page(s)

149-159

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12908799%20AND%20SRC:MED&resulttype=core&format=json

A simple salting out procedure for extracting DNA from human nucleated cells

6 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1081%2FHEM-120023378

Hb Nottingham (alpha2beta2 (FG5) 98 val leads to gly) in a Caucasian male: clinical and biosynthetic studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FHEM-120023378

A new unstable hemoglobin mutated in β 98 (FG 5) Val → Ala: Hb Djelfa

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FHEM-120023378

Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FHEM-120023378

An alpha-thalassemic hemoglobinopathy: homozygosity for the HB Agrinio alpha 2-globin chain variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FHEM-120023378

Haemoglobin Köln (β–98 Valine → Methionine): An Unstable Protein Causing Inclusion-Body Anaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FHEM-120023378

Hb Nottingham or alpha 2 beta 2(98)(FG5)Val----Gly observed as a de novo mutation in a Canadian child

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FHEM-120023378

Characterization of Hb Djelfa [beta98(FG5)Val-->Ala]] by DNA sequencing in a French Caucasian family

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FHEM-120023378

Hb Sun Prairie: diagnostic pitfalls in thalassemic hemoglobinopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FHEM-120023378

Unstable alpha-chain hemoglobin variants with factitious beta-thalassemia biosynthetic ratio: Hb Questembert (alpha 131[H14]Ser-->Pro) and Hb Caen (alpha 132[H15]Val-->Gly)

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FHEM-120023378

Distinct phenotypic expression associated with a new hyperunstable alpha globin variant (Hb heraklion, alpha1cd37(C2)Pro>0): comparison to other alpha-thalassemic hemoglobinopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FHEM-120023378

Compound heterozygosity for two alpha-globin gene defects, Hb Taybe (alpha 1; 38 or 39 minus Thr) and a poly A mutation (alpha 2; AATAAA-->AATAAG), results in a severe hemolytic anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1081%2FHEM-120023378

21 January 2018

Identifiers

DOI

10.1081/HEM-120023378

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12908799%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

1 reference