Hb Bleuland [α108(G15)Thr→Asn, ACC→AAC (α2)]: A New Abnormal Hemoglobin Associated with a Mild α-Thalassemia Phenotype-Reference-Cited by-同舟云学术

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Hb Bleuland [α108(G15)Thr→Asn, ACC→AAC (α2)]: A New Abnormal Hemoglobin Associated with a Mild α-Thalassemia Phenotype

Published:2006-01 Issue:3 Volume:30 Page:349-354
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Harteveld Cornelis L.,Versteegh Florens G.A.,Kok Peter J.M.J.,van Rooijen-Nijdam Irene H.,van Delft Peter,Giordano Piero C.

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.1080/03630260600755351

Reference8 articles.

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

2. Rapid detection of α-thalassaemia deletions and α-globin gene triplication by multiplex polymerase chain reactions

3. Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia

4. Rapid detection of point mutations and polymorphisms of the α-globin genes by DGGE and SSCA

5. Hemoglobin Suan-Dok (α2109(G16)LEU-ARGβ2). an Unstable Variant Associated with α-Thalassemia

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1. In SilicoAnalysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia;Hemoglobin;2020-03-03

2. Hb Nouakchott [α114(GH2)Pro→Leu; HBA1: c.344C>T], A Second and Third Case Described in Two Unrelated Dutch Families;Hemoglobin;2018-01-02

3. Hb Olivet (HBA1: C.40G > A; p.Ala14Thr), a Novel Silent Hemoglobin Variant in Two Families of Distinct Origin;Hemoglobin;2016-09-02

4. Identification of Mutations Causing Aberrant Termination and Deficient Splice Donor Site on theHBA1Gene;Hemoglobin;2015-11-04

5. Molecular Characterization of Hb Hamilton Hill (HBA2: c.388delC), a NovelHBA2Variant Generating a Premature Termination Codon and TruncatedHBA2Chain;Hemoglobin;2015-03-04

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