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Journal Articles

Further characterization of factor VIII-deficient mice created by gene targeting: RNA and protein studies

L Bi, R Sarkar, T Naas, AM Lawler, J Pain, SL Shumaker, V Bedian, HH Jr Kazazian

Blood (1996) 88 (9): 3446–3450.

https://doi.org/10.1182/blood.V88.9.3446.bloodjournal8893446

Published: 1996

Journal Articles

Factor VIII gene inversions in severe hemophilia A: results of an international consortium study

SE Antonarakis, JP Rossiter, M Young, J Horst, P de Moerloose, SS Sommer, RP Ketterling, HH Jr Kazazian, C Negrier, C Vinciguerra

Blood (1995) 86 (6): 2206–2212.

https://doi.org/10.1182/blood.V86.6.2206.bloodjournal8662206

Published: 1995

Journal Articles

Dominant thalassemia-like phenotypes associated with mutations in exon 3 of the beta-globin gene

HH Jr Kazazian, CE Dowling, RL Hurwitz, M Coleman, A Stopeck, JG 3d Adams

Blood (1992) 79 (11): 3014–3018.

https://doi.org/10.1182/blood.V79.11.3014.3014

Published: 1992

Journal Articles

Variation in hemoglobin F production among normal and sickle cell adults is not related to nucleotide substitutions in the gamma promoter regions

EP Economou, SE Antonarakis, HH Jr Kazazian, GR Serjeant, GJ Dover

Blood (1991) 77 (1): 174–177.

https://doi.org/10.1182/blood.V77.1.174.174

Published: 1991

Journal Articles

Characterization of a thrombin cleavage site mutation (Arg 1689 to Cys) in the factor VIII gene of two unrelated patients with cross-reacting material-positive hemophilia A

M Arai, M Higuchi, SE Antonarakis, HH Jr Kazazian, JA 3d Phillips, RL Janco, LW Hoyer

Blood (1990) 75 (2): 384–389.

https://doi.org/10.1182/blood.V75.2.384.384

Published: 1990

Journal Articles

Beta-thalassemia due to two novel nucleotide substitutions in consensus acceptor splice sequences of the beta-globin gene

C Wong, SE Antonarakis, SC Goff, SH Orkin, BG Forget, DG Nathan, PJ Giardina, HH Jr Kazazian

Blood (1989) 73 (4): 914–918.

https://doi.org/10.1182/blood.V73.4.914.914

Published: 1989

Journal Articles

Homozygous beta-thalassemia without anemia

S Safaya, RF Rieder, CE Dowling, HH Jr Kazazian, JG 3d Adams

Blood (1989) 73 (1): 324–328.

https://doi.org/10.1182/blood.V73.1.324.324

Published: 1989

Journal Articles

Molecular basis and prenatal diagnosis of beta-thalassemia

HH Jr Kazazian, CD Boehm

Blood (1988) 72 (4): 1107–1116.

https://doi.org/10.1182/blood.V72.4.1107.1107

Published: 1988

Journal Articles

Molecular characterization of a beta zero-thalassemia resulting from a 1.4 kilobase deletion

R Anand, CD Boehm, HH Jr Kazazian, EF Vanin

Blood (1988) 72 (2): 636–641.

https://doi.org/10.1182/blood.V72.2.636.636

Published: 1988

Journal Articles

The beta-globin gene on the Chinese delta beta-thalassemia chromosome carries a promoter mutation

GF Atweh, XX Zhu, HE Brickner, CH Dowling, HH Jr Kazazian, BG Forget

Blood (1987) 70 (5): 1470–1474.

https://doi.org/10.1182/blood.V70.5.1470.1470

Published: 1987

Journal Articles

A new mutation in IVS-1 of the human beta globin gene causing beta thalassemia due to abnormal splicing

GF Atweh, C Wong, R Reed, SE Antonarakis, D Zhu, PK Ghosh, T Maniatis, BG Forget, HH Jr Kazazian

Blood (1987) 70 (1): 147–151.

https://doi.org/10.1182/blood.V70.1.147.147

Published: 1987

Journal Articles

The spectrum of beta-thalassemia genes in China and Southeast Asia

HH Jr Kazazian, CE Dowling, PG Waber, S Huang, WH Lo

Blood (1986) 68 (4): 964–966.

https://doi.org/10.1182/blood.V68.4.964.964

Published: 1986

Journal Articles

Use of oligonucleotide hybridization in the characterization of a beta zero-thalassemia gene (beta 37 TGG----TGA) in a Saudi Arabian family [published erratum appears in Blood 1986 Jul;68(1):323]

CD Boehm, CE Dowling, PG Waber, PJ Giardina, HH Jr Kazazian

Blood (1986) 67 (4): 1185–1188.

https://doi.org/10.1182/blood.V67.4.1185.1185

Published: 1986

Journal Articles

Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in Greeks

PG Waber, MA Bender, RE Gelinas, C Kattamis, A Karaklis, K Sofroniadou, G Stamatoyannopoulos, FS Collins, BG Forget, HH Jr Kazazian

Blood (1986) 67 (2): 551–554.

https://doi.org/10.1182/blood.V67.2.551.551

Published: 1986

Journal Articles

Concordance of a point mutation 5' to the G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black population

FS Collins, CD Boehm, PG Waber, CJ Jr Stoeckert, SM Weissman, BG Forget, HH Jr Kazazian

Blood (1984) 64 (6): 1292–1296.

https://doi.org/10.1182/blood.V64.6.1292.1292

Published: 1984

Journal Articles

Fetal hemoglobin synthesis in erythroid cultures in hereditary persistence of fetal hemoglobin and beta o-thalassemia

RS Weinberg, SE Antonarakis, HH Jr Kazazian, GJ Dover, SH Orkin, AL Lenes, JM Schofield, BP Alter

Blood (1984) 63 (6): 1278–1284.

https://doi.org/10.1182/blood.V63.6.1278.1278

Published: 1984

Journal Articles

The entire beta-globin gene cluster is deleted in a form of gamma delta beta-thalassemia

ER Fearon, HH Jr Kazazian, PG Waber, JI Lee, SE Antonarakis, SH Orkin, EF Vanin, PS Henthorn, FG Grosveld, AF Scott, GR Buchanan

Blood (1983) 61 (6): 1269–1274.

https://doi.org/10.1182/blood.V61.6.1269.1269

Published: 1983

Journal Articles

Prenatal diagnosis of beta-thalassemias by amniocentesis: linkage analysis using multiple polymorphic restriction endonuclease sites

HH Jr Kazazian, JA 3d Phillips, CD Boehm, TA Vik, MJ Mahoney, AK Ritchey

Blood (1980) 56 (5): 926–930.

https://doi.org/10.1182/blood.V56.5.926.926

Published: 1980

Journal Articles

Unequal crossing-over: a common basis of single alpha-globin genes in Asians and American blacks with hemoglobin-H disease

JA 3d Phillips, TA Vik, AF Scott, KE Young, HH Jr Kazazian, KD Smith, VF Fairbanks, HM Koenig

Blood (1980) 55 (6): 1066–1069.

https://doi.org/10.1182/blood.V55.6.1066.1066

Published: 1980

Journal Articles

A molecular basis for hemoglobin-H disease in American blacks

JA 3d Phillips, AF Scott, KD Smith, KE Young, KL Lightbody, RM Jiji, HH Jr Kazazian

Blood (1979) 54 (6): 1439–1445.

https://doi.org/10.1182/blood.V54.6.1439.1439

Published: 1979

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Further characterization of factor VIII-deficient mice created by gene targeting: RNA and protein studies

Factor VIII gene inversions in severe hemophilia A: results of an international consortium study

Dominant thalassemia-like phenotypes associated with mutations in exon 3 of the beta-globin gene

Variation in hemoglobin F production among normal and sickle cell adults is not related to nucleotide substitutions in the gamma promoter regions

Characterization of a thrombin cleavage site mutation (Arg 1689 to Cys) in the factor VIII gene of two unrelated patients with cross-reacting material-positive hemophilia A

Beta-thalassemia due to two novel nucleotide substitutions in consensus acceptor splice sequences of the beta-globin gene

Homozygous beta-thalassemia without anemia

Molecular basis and prenatal diagnosis of beta-thalassemia

Molecular characterization of a beta zero-thalassemia resulting from a 1.4 kilobase deletion

The beta-globin gene on the Chinese delta beta-thalassemia chromosome carries a promoter mutation

A new mutation in IVS-1 of the human beta globin gene causing beta thalassemia due to abnormal splicing

The spectrum of beta-thalassemia genes in China and Southeast Asia

Use of oligonucleotide hybridization in the characterization of a beta zero-thalassemia gene (beta 37 TGG----TGA) in a Saudi Arabian family [published erratum appears in Blood 1986 Jul;68(1):323]

Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in Greeks

Concordance of a point mutation 5' to the G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black population

Fetal hemoglobin synthesis in erythroid cultures in hereditary persistence of fetal hemoglobin and beta o-thalassemia

The entire beta-globin gene cluster is deleted in a form of gamma delta beta-thalassemia

Prenatal diagnosis of beta-thalassemias by amniocentesis: linkage analysis using multiple polymorphic restriction endonuclease sites

Unequal crossing-over: a common basis of single alpha-globin genes in Asians and American blacks with hemoglobin-H disease

A molecular basis for hemoglobin-H disease in American blacks

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