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Journal Articles

The Brazilian type of nondeletional A gamma-fetal hemoglobin has a C---- G substitution at nucleotide -195 of the A gamma-globin gene

FF Costa, MA Zago, G Cheng, JF Nechtman, TA Stoming, TH Huisman

Blood (1990) 76 (9): 1896–1897.

https://doi.org/10.1182/blood.V76.9.1896.1896

Published: 1990

Journal Articles

A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with “silent” beta-thalassemia

JM Gonzalez-Redondo, TA Stoming, A Kutlar, F Kutlar, KD Lanclos, EF Howard, YJ Fei, M Aksoy, C Altay, A Gurgey

Blood (1989) 73 (6): 1705–1711.

https://doi.org/10.1182/blood.V73.6.1705.1705

Published: 1989

Journal Articles

One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain [letter]

YJ Fei, TA Stoming, A Kutlar, TH Huisman, G Stamatoyannopoulos

Blood (1989) 73 (4): 1075–1077.

https://doi.org/10.1182/blood.V73.4.1075.1075

Published: 1989

Journal Articles

An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin gene

TA Stoming, GS Stoming, KD Lanclos, YJ Fei, C Altay, F Kutlar, TH Huisman

Blood (1989) 73 (1): 329–333.

https://doi.org/10.1182/blood.V73.1.329.329

Published: 1989

Journal Articles

Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States

JM Gonzalez-Redondo, TA Stoming, KD Lanclos, YC Gu, A Kutlar, F Kutlar, T Nakatsuji, B Deng, IS Han, VC McKie

Blood (1988) 72 (3): 1007–1014.

https://doi.org/10.1182/blood.V72.3.1007.1007

Published: 1988

Journal Articles

Identification of base substitutions in the promoter regions of the A gamma- and G gamma-globin genes in A gamma- (or G gamma-) beta+-HPFH heterozygotes using the DNA-amplification-synthetic oligonucleotide procedure

KG Yang, TA Stoming, YJ Fei, S Liang, SC Wong, B Masala, RB Huang, ZP Wei, TH Huisman

Blood (1988) 71 (5): 1414–1417.

https://doi.org/10.1182/blood.V71.5.1414.1414

Published: 1988

Journal Articles

Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes

JC Diaz-Chico, KG Yang, TA Stoming, DG Efremov, A Kutlar, F Kutlar, M Aksoy, C Altay, A Gurgey, Y Kilinc

Blood (1988) 71 (1): 248–251.

https://doi.org/10.1182/blood.V71.1.248.248

Published: 1988

NARROW

The Brazilian type of nondeletional A gamma-fetal hemoglobin has a C---- G substitution at nucleotide -195 of the A gamma-globin gene

A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with “silent” beta-thalassemia

One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain [letter]

An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin gene

Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States

Identification of base substitutions in the promoter regions of the A gamma- and G gamma-globin genes in A gamma- (or G gamma-) beta+-HPFH heterozygotes using the DNA-amplification-synthetic oligonucleotide procedure

Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes

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ASH Publications

American Society of Hematology

The Brazilian type of nondeletional A gamma-fetal hemoglobin has a C---- G substitution at nucleotide -195 of the A gamma-globin gene

A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with “silent” beta-thalassemia

One form of inclusion body beta-thalassemia is due to a GAA----TAA mutation at codon 121 of the beta chain [letter]

An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin gene

Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States

Identification of base substitutions in the promoter regions of the A gamma- and G gamma-globin genes in A gamma- (or G gamma-) beta+-HPFH heterozygotes using the DNA-amplification-synthetic oligonucleotide procedure

Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes

Email alerts

ASH Publications

American Society of Hematology

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