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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

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 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

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

NARROW

Molecular basis and prenatal diagnosis of beta-thalassemia

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

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 G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black population

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

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ASH Publications

American Society of Hematology

Molecular basis and prenatal diagnosis of beta-thalassemia

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

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 G gamma globin gene with G gamma beta +. Hereditary persistence of fetal hemoglobin in the black population

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

Email alerts

ASH Publications

American Society of Hematology

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