David H K Chui

David H K Chui

UNVERIFIED PROFILE

Are you David H K Chui?   Register this Author

Register author
David H K Chui

David H K Chui

Publications by authors named "David H K Chui"

Are you David H K Chui?   Register this Author

100Publications

2009Reads

38Profile Views

An Unusual Case of Low Hemoglobin Oxygen Saturation.

Ann Am Thorac Soc 2019 06;16(6):756-759

4 Department of Internal Medicine, The University of Texas Health Science Center at Houston, Houston, Texas.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1513/AnnalsATS.201811-829CCDOI Listing
June 2019

Inhibition of LSD1 by small molecule inhibitors stimulates fetal hemoglobin synthesis.

Blood 2019 05 16;133(22):2455-2459. Epub 2019 Apr 16.

Section of Hematology-Medical Oncology, Department of Medicine, Boston University School of Medicine, Boston, MA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1182/blood.2018892737DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543516PMC
May 2019

Interference of Hemoglobin A Due to Hemoglobin Franklin Park.

J Appl Lab Med 2019 03 13;3(5):911-913. Epub 2018 Aug 13.

Department of Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1373/jalm.2018.026781DOI Listing
March 2019

Hb Adana (HBA2 or HBA1: c.179G > A) and alpha thalassemia: Genotype-phenotype correlation.

Pediatr Blood Cancer 2018 09 11;65(9):e27220. Epub 2018 May 11.

Boston University School of Medicine, Boston, Massachusetts.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pbc.27220DOI Listing
September 2018

Notch and Aryl Hydrocarbon Receptor Signaling Impact Definitive Hematopoiesis from Human Pluripotent Stem Cells.

Stem Cells 2018 07 1;36(7):1004-1019. Epub 2018 Apr 1.

Section of Hematology and Oncology, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/stem.2822DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099224PMC
July 2018

A Mild Phenotype of Severe β+ Thalassemia in a 16-Month-Old Boy.

J Pediatr Hematol Oncol 2018 04;40(3):e145-e147

Departments of Medicine.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/MPH.0000000000001068DOI Listing
April 2018

A variant Sp1 (R218Q) transcription factor might enhance HbF expression in β -thalassaemia homozygotes.

Br J Haematol 2018 03 27;180(5):755-757. Epub 2017 Feb 27.

Departments of Medicine, Pathology and Laboratory Medicine, Boston University School of Medicine, Boston, MA, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/bjh.14445DOI Listing
March 2018

A long noncoding RNA from the HBS1L-MYB intergenic region on chr6q23 regulates human fetal hemoglobin expression.

Blood Cells Mol Dis 2018 03 29;69:1-9. Epub 2017 Nov 29.

Department of Medicine, Section of Hematology-Oncology, Boston University School of Medicine, Boston, MA 02118, USA; Department of Pathology and Laboratory Medicine, Boston University School of Medicine, Boston, MA 02118, USA. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.bcmd.2017.11.003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783741PMC
March 2018

The clinical severity of hemoglobin S/Black ( γδβ) -thalassemia.

Pediatr Blood Cancer 2017 Nov 28;64(11). Epub 2017 Apr 28.

Department of Hematology, St. Jude Children's Research Hospital, Memphis, Tennessee.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pbc.26596DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615052PMC
November 2017

A Comprehensive, Ethnically Diverse Library of Sickle Cell Disease-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports 2017 04 19;8(4):1076-1085. Epub 2017 Jan 19.

Department of Medicine, Center for Regenerative Medicine (CReM), Boston University School of Medicine, 670 Albany Street, 2nd Floor, Boston, MA 02118, USA; Section of Hematology-Oncology, Department of Medicine, Boston University School of Medicine, Boston, MA 02118, USA. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.stemcr.2016.12.017DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390092PMC
April 2017

Hb Presbyterian (HBB: c.327C>G) in a Nicaraguan Family.

Hemoglobin 2017 Jan 11;41(1):50-52. Epub 2017 Apr 11.

e Department of Medicine and Hemoglobin Diagnostic Reference Laboratory , Boston University School of Medicine , Boston, MA , USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1080/03630269.2017.1302949DOI Listing
January 2017

Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease.

Hemoglobin 2016 15;40(1):64-5. Epub 2015 Sep 15.

a Department of Medicine , Boston University School of Medicine , Boston , Massachusetts , USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3109/03630269.2015.1080725DOI Listing
October 2016

Mild Microcytic Anemia in an Infant with a Compound Heterozygosity for Hb C (HBB: c.19G > A) and Hb Osu Christiansborg (HBB: c.157G > A).

Hemoglobin 2016 Jun;40(3):208-9

d Department of Pediatrics and Department of Molecular , Cell, and Cancer Biology, University of Massachusetts Medical School , Worcester , Massachusetts , USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3109/03630269.2016.1165245DOI Listing
June 2016

Fanconi's Anemia Effect or Sickle Cell Anemia Effect: That is the Question.

Hemoglobin 2015 15;39(4):287-9. Epub 2015 May 15.

Center for Inherited Bone Marrow Failure Syndromes, Hacettepe University , Ankara , Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3109/03630269.2015.1041036DOI Listing
May 2016

Diverse hematological phenotypes of β-thalassemia carriers.

Ann N Y Acad Sci 2016 03 28;1368(1):49-55. Epub 2016 Apr 28.

Departments of Medicine, Pathology, and Laboratory Medicine, Boston University School of Medicine, Boston, Massachusetts.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/nyas.13056DOI Listing
March 2016

Therapeutic fetal-globin inducers reduce transcriptional repression in hemoglobinopathy erythroid progenitors through distinct mechanisms.

Blood Cells Mol Dis 2016 Jan 27;56(1):62-9. Epub 2015 Oct 27.

Hemoglobinopathy Thalassemia Research Unit and Cancer Center, Boston University School of Medicine, Boston, MA, United States; Phoenicia BioSciences, Inc., Newton, MA, United States; Center for Hemoglobin Research in Minorities, Departments of Pediatrics and Medicine, Howard University College of Medicine, Washington DC, United States. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.bcmd.2015.10.004DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4667977PMC
January 2016

The first report of a homozygous codons 9/10 (+T) β-thalassemia mutation in a Turkish patient.

Hemoglobin 2015 9;39(1):66-8. Epub 2015 Jan 9.

Division of Pediatric Hematology, Hacettepe University , Ankara , Turkey.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3109/03630269.2014.982255DOI Listing
September 2015

MALDI-ISD Mass Spectrometry Analysis of Hemoglobin Variants: a Top-Down Approach to the Characterization of Hemoglobinopathies.

J Am Soc Mass Spectrom 2015 Aug 22;26(8):1299-310. Epub 2015 May 22.

Center for Biomedical Mass Spectrometry, Boston University School of Medicine, Boston, MA, 02118, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s13361-015-1164-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4496427PMC
August 2015

Hb Youngstown [β101(G3)Glu → Ala; HBB: c.305A > C]: An unstable hemoglobin variant causing severe hemolytic anemia.

Hemoglobin 2014 27;38(6):381-4. Epub 2014 Oct 27.

Departments of Medicine, and Pathology and Laboratory Medicine, Division of Hematology/Oncology, Boston University School of Medicine , Boston, Massachusetts , USA .

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3109/03630269.2014.971960DOI Listing
July 2015

The genetics of hemoglobin A2 regulation in sickle cell anemia.

Am J Hematol 2014 Nov 4;89(11):1019-23. Epub 2014 Aug 4.

Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajh.23811DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4298130PMC
November 2014

A phase 2 study of HQK-1001, an oral fetal haemoglobin inducer, in β-thalassaemia intermedia.

Br J Haematol 2014 Feb 13;164(3):456-8. Epub 2013 Nov 13.

Lebanese American University, Beirut, Lebanon; Rafik Hariri University Hospital, Beirut, Lebanon.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/bjh.12635DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3904791PMC
February 2014

Sickle cell disease in Saudi Arabia: the phenotype in adults with the Arab-Indian haplotype is not benign.

Br J Haematol 2014 Feb 13;164(4):597-604. Epub 2013 Nov 13.

Department of Paediatrics, Sickle Cell Disease Research Centre, College of Medicine, King Saud University, Riyadh, Saudi Arabia.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/bjh.12650DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4094128PMC
February 2014

Fetal hemoglobin in sickle cell anemia: a glass half full?

Blood 2014 Jan 12;123(4):481-5. Epub 2013 Nov 12.

Center of Excellence in Sickle Cell Disease, Department of Medicine, Boston University School of Medicine, Boston, MA;

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1182/blood-2013-09-528067DOI Listing
January 2014

HbC disorders.

Blood 2013 Nov;122(22):3698

Department of Medicine, Boston University School of Medicine, Center of Excellence for Sickle Cell Disease, Boston Medical Center, Boston, MA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1182/blood-2013-09-526764DOI Listing
November 2013

Novel dominant β-thalassemia: Hb Boston-Kuwait [codon 139/140(+T)].

Pediatr Blood Cancer 2013 Oct 15;60(10):E131-4. Epub 2013 Jun 15.

Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, MA, USA.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/pbc.24611
Publisher Site
http://dx.doi.org/10.1002/pbc.24611DOI Listing
October 2013

Gigantic splenomegaly in a 27-year-old male of South-East Asian descent with concurrent diagnosis of myeloproliferative neoplasm and hemoglobin H disease.

Eur J Haematol 2013 Sep 28;91(3):284-5. Epub 2013 Jun 28.

Department of Pathology, Duke University Medical Center, Durham, NC, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/ejh.12137DOI Listing
September 2013

Hemoglobin Shady Grove: a novel fetal methemoglobin variant.

Pediatr Blood Cancer 2013 Aug 4;60(8):E55-6. Epub 2013 Mar 4.

Department of Hematology/Oncology, Children's National Medical Center, Michigan Ave, Washington, District of Columbia 20010, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pbc.24503DOI Listing
August 2013

Massive splenic infarction in an adolescent with hemoglobin S-HPFH.

Pediatr Blood Cancer 2013 Jul 31;60(7):E49-51. Epub 2012 Dec 31.

Yale University School of Medicine, New Haven, Connecticut, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pbc.24444DOI Listing
July 2013

Severe fetal and neonatal hemolytic anemia due to a 198 kb deletion removing the complete β-globin gene cluster.

Pediatr Blood Cancer 2012 Nov 31;59(5):941-4. Epub 2012 Jan 31.

Hematology/Oncology, Department of Medicine, Boston University School of Medicine, Boston, MA, USA.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/pbc.24094
Publisher Site
http://dx.doi.org/10.1002/pbc.24094DOI Listing
November 2012

Compound heterozygosity for Hb S [β6(A3)Glu→Val] and Hb Kenya (Aγ81Leu-β86Ala) in a Ugandan woman.

Hemoglobin 2012 2;36(3):270-5. Epub 2012 Mar 2.

Quest Diagnostics Nichols Institute, 14225 Newbrook Drive, Chantilly, VA, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3109/03630269.2012.658483DOI Listing
October 2012

Pulse oximetry screening for critical congenital heart defects.

Lancet 2012 Oct;380(9850):1305-6; author reply 1306

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/S0140-6736(12)61754-1DOI Listing
October 2012

Fetal hemoglobin in sickle cell anemia: molecular characterization of the unusually high fetal hemoglobin phenotype in African Americans.

Am J Hematol 2012 Feb 3;87(2):217-9. Epub 2011 Dec 3.

Division of Hematology/Oncology, Department of Medicine, Boston University School of Medicine, Boston, MA, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajh.22221DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3302931PMC
February 2012

Is HbA2 level a reliable diagnostic measurement for β-thalassemia trait in people with iron deficiency?

Am J Hematol 2012 Jan 31;87(1):114-6. Epub 2011 Oct 31.

Department of Medicine, Boston University School of Medicine, Massachusetts, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajh.22188DOI Listing
January 2012

New and known β-thalassemia determinants masked by known and new δ gene defects [Hb A(2)-Ramallah or δ6(A3)Glu→Gln, GAG>CAG].

Hemoglobin 2010 ;34(5):445-50

The Reference Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3109/03630269.2010.511591DOI Listing
March 2011

Unexpectedly low pulse oximetry measurements associated with variant hemoglobins: a systematic review.

Am J Hematol 2010 Nov;85(11):882-5

Section of Hematology and Oncology, Department of Medicine, Boston University School of Medicine, Boston, MA 02118, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajh.21810DOI Listing
November 2010

Fetal globin gene inducers: novel agents and new potential.

Ann N Y Acad Sci 2010 Aug;1202:158-64

Cancer Center and Hemoglobinopathy-Thalassemia Research Unit, Department of Medicine, Pediatrics, Pharmacology and Experimental Therapeutics, Boston University School of Medicine, Boston, Massachusetts, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1749-6632.2010.05593.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3913055PMC
August 2010

BCL11A represses HBG transcription in K562 cells.

Blood Cells Mol Dis 2009 Mar-Apr;42(2):144-9. Epub 2009 Jan 18.

Center of Excellence in Sickle Cell Disease, Division of Hematology/Oncology, Department of Medicine, Boston University School of Medicine, Boston, MA 02118, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.bcmd.2008.12.003DOI Listing
May 2009

Hemoglobin Kenya composed of alpha- and ((A)gammabeta)-fusion-globin chains, associated with hereditary persistence of fetal hemoglobin.

Am J Hematol 2009 Jan;84(1):55-8

Hemoglobin Diagnostic Reference Laboratory, Boston Medical Center, Boston, MA 02118, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajh.21308DOI Listing
January 2009

BCL11A is a major HbF quantitative trait locus in three different populations with beta-hemoglobinopathies.

Blood Cells Mol Dis 2008 Nov-Dec;41(3):255-258. Epub 2008 Aug 8.

Division of Hematology/Oncology, Center of Excellence in Sickle Cell Disease, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.bcmd.2008.06.007DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4100606PMC
November 2008

A T-to-G transversion at nucleotide -567 upstream of HBG2 in a GATA-1 binding motif is associated with elevated hemoglobin F.

Mol Cell Biol 2008 Jul 28;28(13):4386-93. Epub 2008 Apr 28.

Center of Excellence in Sickle Cell Disease, Division of Hematology/Oncology, Department of Medicine, Boston University School of Medicine, Boston, Massachusetts 02118, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1128/MCB.00071-08DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2447137PMC
July 2008

Beta-thalassemia intermedia due to compound heterozygosity for two beta-globin gene promoter mutations, including a novel TATA box deletion.

Pediatr Blood Cancer 2008 Feb;50(2):363-6

Hemoglobin Diagnostic Reference Laboratory, Boston Medical Center, Boston, Massachusetts, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pbc.20916DOI Listing
February 2008

Sickle cell disease caused by Hb S/Québec-CHORI: treatment with hydroxyurea and response.

Pediatr Blood Cancer 2007 Aug;49(2):207-10

Department of Medicine, Children's Hospital Boston, Boston, Massachusetts 02115, USA.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/pbc.21269
Publisher Site
http://dx.doi.org/10.1002/pbc.21269DOI Listing
August 2007

Hemoglobin SE disease: a concise review.

Am J Hematol 2007 Jul;82(7):643-9

The Center of Excellence in Sickle Cell Disease, Department of Medicine, School of Medicine, Boston University, Boston, MA, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajh.20847DOI Listing
July 2007

Two new alpha-thalassemia frameshift mutations.

Hemoglobin 2007 ;31(2):135-9

Hemoglobin Diagnostic Reference Laboratory, Boston Medical Center, Boston, Massachusetts 02118, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1080/03630260701285118DOI Listing
July 2007

HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update.

Hum Mutat 2007 Feb;28(2):206

The Pennsylvania State University, Center for Comparative Genomics and Bioinformatics, University Park, Pennsylvania, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/humu.9479DOI Listing
February 2007

Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7-kb beta-globin gene deletion.

Eur J Haematol 2007 Jan 13;78(1):82-5. Epub 2006 Oct 13.

Hemoglobin Diagnostic Reference Laboratory, Boston Medical Center, Boston, MA 02118, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1600-0609.2006.00771.xDOI Listing
January 2007

Alpha-thalassemia: Hb H disease and Hb Barts hydrops fetalis.

Authors:
David H K Chui

Ann N Y Acad Sci 2005 ;1054:25-32

Department of Medicine and Pathology, Boston University School of Medicine, 88 East Newton Street, Boston, MA 02118, USA.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1196/annals.1345.004
Publisher Site
http://dx.doi.org/10.1196/annals.1345.004DOI Listing
July 2006

Prenatal diagnosis of hemoglobinopathies in Ontario, Canada.

Ann N Y Acad Sci 2005 ;1054:507-10

Department of Pathology and Molecular Medicine, Faculty of Health Sciences, McMaster University Medical Centre, 1200 Main Street West, Hamilton, Ontario L8N 3Z5, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1196/annals.1345.052DOI Listing
July 2006

Hemoglobinopathies mimicking Hb S/beta-thalassemia: Hb S/S with alpha-thalassemia and Hb S/Volga.

Am J Hematol 2006 May;81(5):361-5

Hemoglobin Diagnostic Reference Laboratory, Boston Medical Center, Boston, Massachusetts 02118, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajh.20562DOI Listing
May 2006

Determining the cause of patchwork HBA1 and HBA2 genes: recurrent gene conversion or crossing over fixation events.

Haematologica 2006 Mar 17;91(3):297-302. Epub 2006 Feb 17.

Department of Pediatric Medicine, KK Women's & Children's Hospital, Singapore.

View Article

Download full-text PDF

Source
March 2006

Alpha-thalassaemia and population health in Southeast Asia.

Authors:
David H K Chui

Ann Hum Biol 2005 Mar-Apr;32(2):123-30

Department of Medicine, Boston University School of Medicine, Boston, Massachusetts 02118, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1080/03014460500075084DOI Listing
December 2005

Hb Hope [beta136(H14)Gly-->Asp (GGT-->GAT)]: interactions with Hb S [beta6(A3)Glu-->Val (GAG-->GTG)], other variant hemoglobins and thalassemia.

Hemoglobin 2004 ;28(4):277-85

Department of Medicine and Pathology, Division of Hematology/Oncology, Boston University School of Medicine, Boston, Massachusetts, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1081/hem-200037801DOI Listing
May 2005

Simple non-invasive prenatal detection of Hb Bart's disease by analysis of fetal erythrocytes in maternal blood.

Prenat Diagn 2005 Feb;25(2):123-8

Prenatal Diagnostic and Counselling Department, Tsan Yuk Hospital, Hong Kong.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pd.1096DOI Listing
February 2005

Hemoglobin Titusville, a low oxygen affinity variant hemoglobin, in a family of Northern European background.

Am J Hematol 2004 Dec;77(4):384-6

Hemoglobin Diagnostic Reference Laboratory, Boston Medical Center, Boston, Massachusetts 02118, USA.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/ajh.20209
Publisher Site
http://dx.doi.org/10.1002/ajh.20209DOI Listing
December 2004

A novel sickle hemoglobin: hemoglobin S-south end.

J Pediatr Hematol Oncol 2004 Nov;26(11):773-6

Hemoglobin Diagnostic Reference Laboratory, Boston Medical Center, Boston, Massachusetts, USA.

View Article

Download full-text PDF

Source
http://pdfs.journals.lww.com/jpho-online/2004/11000/A_Novel_
Web Search
http://dx.doi.org/10.1097/00043426-200411000-00019DOI Listing
November 2004

Good practice guidelines for laboratory investigation of hemoglobinopathies.

Lab Hematol 2003 ;9(4):237-45

Provincial Hemoglobinopathy Laboratory, Hamilton Regional Laboratory Medicine Program, Hamilton, Ontario, Canada.

View Article

Download full-text PDF

Source
August 2004

Development of primitive and definitive hematopoiesis from nonhuman primate embryonic stem cells in vitro.

Development 2004 Apr;131(8):1869-79

Department of Pediatrics, Graduate School of Medicine, Kyoto University, 54 Kawahara-cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1242/dev.01065DOI Listing
April 2004

Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies.

Nucleic Acids Res 2004 Jan;32(Database issue):D537-41

MGC-Department of Cell Biology and Genetics, Erasmus MC, Faculty of Medicine and Health Sciences, PO Box 1738, 3000 DR, Rotterdam, The Netherlands.

View Article

Download full-text PDF

Source
https://academic.oup.com/nar/article-lookup/doi/10.1093/nar/
Publisher Site
http://dx.doi.org/10.1093/nar/gkh006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC308741PMC
January 2004

Single-tube multiplex-PCR screen for anti-3.7 and anti-4.2 alpha-globin gene triplications.

Clin Chem 2003 Oct;49(10):1679-82

Department of Pediatrics, National University of Singapore, Singapore 119074, Singapore.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1373/49.10.1679DOI Listing
October 2003

Identification of a new hemoglobin variant: Hb St. Joseph's [beta77(EF1)His-->Leu].

Hemoglobin 2003 Aug;27(3):181-3

Hamilton Regional Laboratory Medicine Program, Hamilton, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1081/hem-120023382DOI Listing
August 2003

Identification of a new beta-thalassemia nonsense mutation [codon 59 (AAG-->TAG)].

Hemoglobin 2003 Aug;27(3):201-3

Hamilton Regional Laboratory Medicine Program, Hamilton, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1081/hem-120023385DOI Listing
August 2003

Multiple minisequencing screen for seven southeast Asian nondeletional alpha-thalassemia mutations.

Clin Chem 2003 May;49(5):800-3

Departments of. Pediatrics and Obstetrics & Gynecology, National University of Singapore 119074, Singapore.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1373/49.5.800DOI Listing
May 2003

Hemoglobin H disease: not necessarily a benign disorder.

Blood 2003 Feb 12;101(3):791-800. Epub 2002 Sep 12.

Department of Pathology and Molecular Medicine, McMaster University Faculty of Health Sciences, Hamilton, ON, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1182/blood-2002-07-1975DOI Listing
February 2003

Evaluation of a dual hemoglobin A(2)/A(1c) quantitation kit on the bio-rad variant II automated hemoglobin analyzer.

Arch Pathol Lab Med 2002 Dec;126(12):1494-500

Hamilton Regional Laboratory Medicine Program, Hamilton, Ontario, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1043/0003-9985(2002)126<1494:EOADHA>2.0.CO;2DOI Listing
December 2002