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Works (20)

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

2013-06-15 | Standards or policy
DOI:

10.1002/pbc.24611

PMID:

23776097
Source: Self-asserted source
Hong Luo

Fetal hemoglobin in sickle cell anemia: Genetic studies of the Arab-Indian haplotype.

2013-03-07 | Standards or policy
DOI:

10.1016/j.bcmd.2012.12.005

PMID:

23465615
Source: Self-asserted source
Hong Luo

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

2012-01-31 | Standards or policy
DOI:

10.1002/pbc.24094

PMID:

22294483
Source: Self-asserted source
Hong Luo

Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobin.

2011-10-24 | Standards or policy
DOI:

10.1111/j.1365-2141.2011.08916.x

PMID:

22017641
Source: Self-asserted source
Hong Luo

A 3-bp deletion in the HBS1L-MYB intergenic region on chromosome 6q23 is associated with HbF expression.

2011-03-08 | Standards or policy
DOI:

10.1182/blood-2010-11-317081

PMID:

21385855
Source: Self-asserted source
Hong Luo

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

2010-11-01 | Standards or policy
DOI:

10.1002/ajh.21810

PMID:

20890907
Source: Self-asserted source
Hong Luo

New and known ß-thalassemia determinants masked by known and new d gene defects [Hb A(2)-Ramallah or d6(A3)Glu?Gln, GAG>>CAG].

2010-01-01 | Standards or policy
DOI:

10.3109/03630269.2010.511591

PMID:

20854118
Source: Self-asserted source
Hong Luo

Sickle cell disease caused by heterozygosity for Hb S and novel LCR deletion: Report of two patients.

2009-09-01 | Standards or policy
DOI:

10.1002/ajh.21480

PMID:

19650141
Source: Self-asserted source
Hong Luo

BCL11A represses HBG transcription in K562 cells.

2009-01-18 | Standards or policy
DOI:

10.1016/j.bcmd.2008.12.003

PMID:

19153051
Source: Self-asserted source
Hong Luo

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

2009-01-01 | Standards or policy
DOI:

10.1002/ajh.21308

PMID:

19006227
Source: Self-asserted source
Hong Luo

Mutations in the paralogous human alpha-globin genes yielding identical hemoglobin variants.

2008-10-16 | Standards or policy
DOI:

10.1007/s00277-008-0624-3

PMID:

18923834
Source: Self-asserted source
Hong Luo

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

2008-04-28 | Standards or policy
DOI:

10.1128/MCB.00071-08

PMID:

18443038
Source: Self-asserted source
Hong Luo

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

2008-02-01 | Standards or policy
DOI:

10.1002/pbc.20916

PMID:

16732578
Source: Self-asserted source
Hong Luo

Two new alpha-thalassemia frameshift mutations.

2007-01-01 | Standards or policy
DOI:

10.1080/03630260701285118

PMID:

17486494
Source: Self-asserted source
Hong Luo

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

2006-10-13 | Standards or policy
DOI:

10.1111/j.1600-0609.2006.00771.x

PMID:

17038017
Source: Self-asserted source
Hong Luo

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

2006-05-01 | Standards or policy
DOI:

10.1002/ajh.20562

PMID:

16628724
Source: Self-asserted source
Hong Luo

Dominantly inherited beta thalassaemia intermedia caused by a new single nucleotide deletion in exon 2 of the beta globin gene: Hb morgantown (beta91 CTG>CG).

2005-10-01 | Standards or policy
DOI:

10.1136/jcp.2004.023010

PMID:

16189162
Source: Self-asserted source
Hong Luo

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

2004-12-01 | Standards or policy
DOI:

10.1002/ajh.20209

PMID:

15551405
Source: Self-asserted source
Hong Luo

A novel sickle hemoglobin: hemoglobin S-south end.

2004-11-01 | Standards or policy
DOI:

10.1097/00043426-200411000-00019

PMID:

15543018
Source: Self-asserted source
Hong Luo

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

2004-01-01 | Standards or policy
DOI:

10.1081/HEM-200037801

PMID:

15658184
Source: Self-asserted source
Hong Luo
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