Search details
1.
Eleven Cases of Hb J-Paris-I [HBA2: c.38C>A (or HBA1)]: A Stable α Chain Variant Elutes in the P3 Window on High-Performance Liquid Chromatography.
Hemoglobin
; 45(5): 322-324, 2021 Sep.
Article
in English
| MEDLINE | ID: mdl-34784833
2.
Eight Cases of Hb Winnipeg [HBA2: c.226G>T (or HBA1)]: A Detailed Study.
Hemoglobin
; 45(4): 256-258, 2021 Jul.
Article
in English
| MEDLINE | ID: mdl-34496687
3.
Hb Calgary (HBB: c.194G>T): A Highly Unstable Hemoglobin Variant with a ß-Thalassemia Major Phenotype.
Hemoglobin
; 45(4): 215-219, 2021 Jul.
Article
in English
| MEDLINE | ID: mdl-34311670
4.
Fifteen Cases of Hb J-Meerut: The Rare Association with Hb E and/or HBA1: c.-24C>G (or HBA2) Variants.
Hemoglobin
; 44(5): 364-367, 2020 Sep.
Article
in English
| MEDLINE | ID: mdl-32924661
5.
Twelve Cases of Hb Manitoba [α102(G9)SerâArg]: the Fluctuation in the Variant Expression.
Hemoglobin
; 44(6): 442-445, 2020 Nov.
Article
in English
| MEDLINE | ID: mdl-33249879
6.
A Wide Spectrum Study of α-Globin Chain Variants: Cases from the UK.
Hemoglobin
; 44(3): 195-200, 2020 May.
Article
in English
| MEDLINE | ID: mdl-32597250
7.
SAMHD1 is mutated recurrently in chronic lymphocytic leukemia and is involved in response to DNA damage.
Blood
; 123(7): 1021-31, 2014 Feb 13.
Article
in English
| MEDLINE | ID: mdl-24335234
8.
Ten Years of Routine α- and ß-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations.
Hemoglobin
; 40(2): 75-84, 2016.
Article
in English
| MEDLINE | ID: mdl-26635043
9.
Characterization of Hb Lepore variants in the UK population.
Hemoglobin
; 39(1): 58-61, 2015.
Article
in English
| MEDLINE | ID: mdl-25490067
10.
Prenatal diagnosis of hemoglobinopathies by pyrosequencing: a more sensitive and rapid approach to fetal genotyping.
Hemoglobin
; 36(2): 144-50, 2012.
Article
in English
| MEDLINE | ID: mdl-22239406
11.
Characterization of a novel deletion causing beta-thalassemia major in an Afghan family.
Hemoglobin
; 34(1): 110-4, 2010.
Article
in English
| MEDLINE | ID: mdl-20113295
12.
Multiplex ligation-dependent probe amplification identification of 17 different beta-globin gene deletions (including four novel mutations) in the UK population.
Hemoglobin
; 33(6): 406-16, 2009.
Article
in English
| MEDLINE | ID: mdl-19958185
13.
The accurate prediction of rare hemoglobin variants using a combination of high performance liquid chromatography, retention time and isoelectric focusing electrophoresis position.
Saudi Med J
; 30(9): 1158-64, 2009 Sep.
Article
in English
| MEDLINE | ID: mdl-19750260
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