189 related articles for article (PubMed ID: 3942832)
1. A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait.
Steinberg MH; Coleman MB; Adams JG; Hartmann RC; Saba H; Anagnou NP
Blood; 1986 Feb; 67(2):469-73. PubMed ID: 3942832
[TBL] [Abstract][Full Text] [Related]
2. Modification of hemoglobin H disease by sickle trait.
Matthay KK; Mentzer WC; Dozy AM; Kan YW; Bainton DF
J Clin Invest; 1979 Oct; 64(4):1024-32. PubMed ID: 479366
[TBL] [Abstract][Full Text] [Related]
3. Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin gene.
Steinberg MH; Embury SH
Blood; 1986 Nov; 68(5):985-90. PubMed ID: 3533181
[TBL] [Abstract][Full Text] [Related]
4. A molecular basis for hemoglobin-H disease in American blacks.
Phillips JA; Scott AF; Smith KD; Young KE; Lightbody KL; Jiji RM; Kazazian HH
Blood; 1979 Dec; 54(6):1439-45. PubMed ID: 508947
[TBL] [Abstract][Full Text] [Related]
5. Gene mapping of Malaysian alpha thalassemias with alpha and zeta globin gene probes.
Lie-Injo LE; Herrera AR; Lebo RV; Hassan K; Lopez CG
Am J Hematol; 1985 Mar; 18(3):289-96. PubMed ID: 2983536
[TBL] [Abstract][Full Text] [Related]
6. Unequal crossing-over: a common basis of single alpha-globin genes in Asians and American blacks with hemoglobin-H disease.
Phillips JA; Vik TA; Scott AF; Young KE; Kazazian HH; Smith KD; Fairbanks VF; Koenig HM
Blood; 1980 Jun; 55(6):1066-9. PubMed ID: 6246995
[TBL] [Abstract][Full Text] [Related]
7. Alpha-thalassemia in blacks: interactions with the sickle hemoglobin gene.
Steinberg MH; Embury SH
Birth Defects Orig Artic Ser; 1987; 23(5A):43-8. PubMed ID: 3689929
[No Abstract] [Full Text] [Related]
8. Dysfunctional alpha-globin genes in hemoglobin H disease in blacks: variation in restriction fragment size permits the detection of the -alpha/-alpha T genotype.
Safaya S; Mullaney P; Rieder RF
Am J Hematol; 1987 Dec; 26(4):329-39. PubMed ID: 2891296
[TBL] [Abstract][Full Text] [Related]
9. Alpha-thalassemia in blacks is due to gene deletion.
Davis JR; Dozy AM; Lubin B; Koenig HM; Pierce HI; Stamatoyannopoulos G; Kan YW
Am J Hum Genet; 1979 Sep; 31(5):569-73. PubMed ID: 507051
[TBL] [Abstract][Full Text] [Related]
10. Organization of alpha-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, beta-thalassemia, and alpha-thalassemia-2.
Felice AE; Ozdonmez R; Headlee ME; Huisman TH
Biochem Genet; 1982 Aug; 20(7-8):689-701. PubMed ID: 6291506
[No Abstract] [Full Text] [Related]
11. Mapping the alpha-globin genes in an Algerian HbH patient and his family.
Whitelaw E; Pagnier J; Verdier G; Henni T; Godet J; Williamson R
Blood; 1980 Mar; 55(3):511-6. PubMed ID: 7357081
[TBL] [Abstract][Full Text] [Related]
12. Molecular basis for HbH disease in Italy: geographical distribution of deletional and nondeletional alpha-thalassemia haplotypes.
Di Rienzo A; Novelletto A; Aliquò MC; Bianco I; Tagarelli A; Brancati C; Colombo B; Felicetti L
Am J Hum Genet; 1986 Nov; 39(5):631-9. PubMed ID: 2878610
[TBL] [Abstract][Full Text] [Related]
13. Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia.
Honig GR; Gunay U; Mason RG; Vida LN; Ferenc C
Pediatr Res; 1976 Jun; 10(6):613-20. PubMed ID: 1272638
[TBL] [Abstract][Full Text] [Related]
14. The rare alpha-thalassemia-1 of blacks is a zeta alpha-thalassemia-1 associated with deletion of all alpha- and zeta-globin genes.
Felice AE; Cleek MP; McKie K; McKie V; Huisman TH
Blood; 1984 May; 63(5):1253-7. PubMed ID: 6713099
[TBL] [Abstract][Full Text] [Related]
15. Partial deletion of the alpha-globin structural gene in human alpha-thalassaemia.
Orkin SH; Michelson A
Nature; 1980 Jul; 286(5772):538-40. PubMed ID: 7402334
[No Abstract] [Full Text] [Related]
16. The varied arrangement of the alpha globin genes in alpha thalassemia and Hb H disease in American blacks.
Sancar GB; Cedeno MM; Rieder RF
Johns Hopkins Med J; 1980 Jun; 146(6):264-9. PubMed ID: 6155503
[TBL] [Abstract][Full Text] [Related]
17. Sickle cell anemia associated with alpha-thalassemia in Malaysian Indians.
Lie-Injo LE; Hassan K; Joishy SK; Lim ML
Am J Hematol; 1986 Jul; 22(3):265-74. PubMed ID: 2424302
[TBL] [Abstract][Full Text] [Related]
18. [Study of the molecular causes of thalassemia. II. Deletion of alpha-globin genes in hemoglobinopathy H].
Shipitsyna GI; Lunts MG; Shifter KA; Idel'son LI; Limborskaia SA
Genetika; 1980; 16(1):78-85. PubMed ID: 6449401
[TBL] [Abstract][Full Text] [Related]
19. Identification of a nondeletion defect in alpha-thalassemia.
Kan YW; Dozy AM; Trecartin R; Todd D
N Engl J Med; 1977 Nov; 297(20):1081-4. PubMed ID: 909565
[TBL] [Abstract][Full Text] [Related]
20. The molecular basis of alpha-thalassaemia in Thailand.
Winichagoon P; Higgs DR; Goodbourn SE; Clegg JB; Weatherall DJ; Wasi P
EMBO J; 1984 Aug; 3(8):1813-8. PubMed ID: 6548185
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]