Waber PG - Search Results

1

Quantification of the close association between DNA haplotypes and specific beta-thalassaemia mutations in Mediterraneans.

Kazazian HH Jr, Orkin SH, Markham AF, Chapman CR, Youssoufian H, Waber PG. Kazazian HH Jr, et al. Among authors: waber pg. Nature. 1984 Jul 12-18;310(5973):152-4. doi: 10.1038/310152a0. Nature. 1984. PMID: 6738712

2

Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster.

Orkin SH, Kazazian HH Jr, Antonarakis SE, Goff SC, Boehm CD, Sexton JP, Waber PG, Giardina PJ. Orkin SH, et al. Among authors: waber pg. Nature. 1982 Apr 15;296(5858):627-31. doi: 10.1038/296627a0. Nature. 1982. PMID: 6280057 No abstract available.

3

Use of haplotype analysis in the beta-globin gene cluster to discover beta-thalassemia mutations.

Kazazian HH Jr, Antonarakis SE, Cheng T, Boehm CD, Waber PG. Kazazian HH Jr, et al. Among authors: waber pg. Prog Clin Biol Res. 1983;134:91-8. Prog Clin Biol Res. 1983. PMID: 6665005

4

Molecular characterization of seven beta-thalassemia mutations in Asian Indians.

Kazazian HH Jr, Orkin SH, Antonarakis SE, Sexton JP, Boehm CD, Goff SC, Waber PG. Kazazian HH Jr, et al. Among authors: waber pg. EMBO J. 1984 Mar;3(3):593-6. doi: 10.1002/j.1460-2075.1984.tb01853.x. EMBO J. 1984. PMID: 6714226 Free PMC article.

5

Use of oligonucleotide hybridization in the characterization of a beta zero-thalassemia gene (beta 37 TGG----TGA) in a Saudi Arabian family.

Boehm CD, Dowling CE, Waber PG, Giardina PJ, Kazazian HH Jr. Boehm CD, et al. Among authors: waber pg. Blood. 1986 Apr;67(4):1185-8. Blood. 1986. PMID: 3006832 Free article.

6

Beta-thalassemia in China: a systematic molecular characterization of beta-thalassemia mutations.

Huang S, Waber PG, Dowling CE, Wong C, Antonarakis SE, Cai RL, Wang MQ, Lo WH, Kazazian HH Jr. Huang S, et al. Among authors: waber pg. Hemoglobin. 1988;12(5-6):621-8. doi: 10.3109/03630268808991653. Hemoglobin. 1988. PMID: 3209404

7

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

Fearon ER, Kazazian HH Jr, Waber PG, Lee JI, Antonarakis SE, Orkin SH, Vanin EF, Henthorn PS, Grosveld FG, Scott AF, Buchanan GR. Fearon ER, et al. Among authors: waber pg. Blood. 1983 Jun;61(6):1269-74. Blood. 1983. PMID: 6839025 Free article.

8

Beta-thalassemia in Chinese--analysis of polymorphic restriction site haplotypes in the beta-globin gene cluster.

Huang SZ, Kazazian HH Jr, Waber PG, Luo HY, Cai RL, Wang MQ. Huang SZ, et al. Among authors: waber pg. Chin Med J (Engl). 1985 Dec;98(12):881-6. Chin Med J (Engl). 1985. PMID: 3009101 No abstract available.

9

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.

Collins FS, Boehm CD, Waber PG, Stoeckert CJ Jr, Weissman SM, Forget BG, Kazazian HH Jr. Collins FS, et al. Among authors: waber pg. Blood. 1984 Dec;64(6):1292-6. Blood. 1984. PMID: 6208955 Free article.

10

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

Waber PG, Bender MA, Gelinas RE, Kattamis C, Karaklis A, Sofroniadou K, Stamatoyannopoulos G, Collins FS, Forget BG, Kazazian HH Jr. Waber PG, et al. Blood. 1986 Feb;67(2):551-4. Blood. 1986. PMID: 2417646 Free article.

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