Hb Taybe: Description of genetics and laboratory findings in an Israeli Arab family

被引：5

作者：

Ben-Bassat, I ^{[1
]}

Simjanovska, L

Jaber, L

Efremov, GD

机构：

[1] Chaim Sheba Med Ctr, Inst Hematol, IL-52621 Tel Hashomer, Israel

[2] Tel Aviv Univ, Sackler Sch Med, IL-52621 Tel Hashomer, Israel

[3] Macedonian Acad Sci & Arts, Res Ctr Genet Engn & Biotechnol, Skopje 91000, Macedonia

来源：

HEMOGLOBIN | 1998年 / 22卷 / 02期

关键词：

D O I：

10.3109/03630269809092141

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

[No abstract available]

引用

页码：161 / 166

页数：6

共 7 条

[1]

BENBASSAT I, 1969, ISRAEL J MED SCI, V5, P383

[2] HB ADANA OR ALPHA(2)59(E8)GLY-]ASP-BETA(2), A SEVERELY UNSTABLE ALPHA(1)-GLOBIN VARIANT, OBSERVED IN COMBINATION WITH THE -(ALPHA)20.5 KB ALPHA-THAL-1 DELETION IN 2 TURKISH PATIENTS [J].

CURUK, MA ;

DIMOVSKI, AJ ;

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GU, LH ;

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ALTAY, C ;

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HUISMAN, THJ .

AMERICAN JOURNAL OF HEMATOLOGY, 1993, 44 (04) :270-275

[3]

GALACTEROS F, 1994, CR ACAD SCI III-VIE, V317, P437

[4]

Girodon EMRA, 1992, BLOOD S, V80, p388a

[5] COMPOUND HETEROZYGOSITY FOR 2 ALPHA-GLOBIN GENE DEFECTS, HB-TAYBE (ALPHA-1, 38 OR 39 MINUS THR) AND A POLY A MUTATION (ALPHA-2, AATAA(A)UNDER-BAR-]AATAA(G)UNDER-BAR), RESULTS IN A SEVERE HEMOLYTIC-ANEMIA [J].

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MOLCHANOVA, TP ;

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HUISMAN, THJ .

AMERICAN JOURNAL OF HEMATOLOGY, 1994, 47 (03) :198-202

[6]

Rees DC, 1997, BLOOD, V90, P2823

[7] UNSTABLE ALPHA-CHAIN HEMOGLOBIN-VARIANTS WITH FACTITIOUS BETA-THALASSEMIA BIOSYNTHETIC RATIO - HB QUESTEMBERT (ALPHA-131[H14] SER-]PRO) AND HB CAEN (ALPHA-132[H15] VAL-]GLY) [J].

WAJCMAN, H ;

VASSEUR, C ;

BLOUQUIT, Y ;

ROSA, J ;

LABIE, D ;

NAJMAN, A ;

REMAN, O ;

LEPORRIER, M ;

GALACTEROS, F .

AMERICAN JOURNAL OF HEMATOLOGY, 1993, 42 (04) :367-374

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