119 related articles for article (PubMed ID: 10722119)
1. Hb Siam [alpha15(A13)Gly-->Arg] is a GGT-->CGT mutation in the alpha1-globin gene.
Yodsowan B; Svast J; Srisomsap C; Winichagoon P; Fucharoen S
Hemoglobin; 2000 Feb; 24(1):71-5. PubMed ID: 10722119
[No Abstract] [Full Text] [Related]
2. Hb Siam [alpha15(A13)Gly-->Arg (alpha1) (GGT-->CGT)] is a typical alpha chain hemoglobinopathy without an alpha-thalassemic effect.
Turbpaiboon C; Svasti S; Sawangareetakul P; Winichagoon P; Srisomsap C; Siritanaratkul N; Fucharoen S; Wilairat P; Svasti J
Hemoglobin; 2002 Feb; 26(1):77-81. PubMed ID: 11939517
[No Abstract] [Full Text] [Related]
3. Hb Ube-2 in a Taiwanese subject: an A-->G substitution at codon 68 of the alpha2-globin gene.
Shin MC; Chen CM; Liu SC; Huang CH; Lee TP; Chan WL; Chang JG
Hemoglobin; 2002 Feb; 26(1):99-101. PubMed ID: 11939522
[No Abstract] [Full Text] [Related]
4. Molecular and clinical characteristics of hemoglobin Ottawa detected in a Chinese population.
Huang Y; Lin M; Lin CP; Wu JR; Zheng LH; Yang LY
Mol Med Rep; 2011; 4(3):581-3. PubMed ID: 21468611
[TBL] [Abstract][Full Text] [Related]
5. Hb Kurosaki [alpha7(A5)Lys -->Glu (AAG --> GAG)]: an alpha2-globin gene mutation found in Thailand.
Ngiwsara L; Srisomsap C; Winichagoon P; Fucharoen S; Sae-Ngow B; Svasti J
Hemoglobin; 2005; 29(2):155-9. PubMed ID: 15921168
[TBL] [Abstract][Full Text] [Related]
6. A novel mutation of the alpha2-globin causing alpha(+)-thalassemia: Hb Plasencia [alpha125(H8)Leu--Arg (alpha2).
Martin G; Villegas A; González FA; Ropero P; Hojas R; Polo M; Mateo M; Salvador M; Benavente C
Hemoglobin; 2005; 29(2):113-7. PubMed ID: 15921163
[TBL] [Abstract][Full Text] [Related]
7. Hb Manitoba in a Taiwanese family: a C-->A substitution at codon 102 of the alpha2-globin gene.
Chang JG; Shih MC; Liu SC; Chan WL; Peng CT
Hemoglobin; 2001 Nov; 25(4):437-9. PubMed ID: 11791879
[No Abstract] [Full Text] [Related]
8. A new highly unstable alpha chain variant causing alpha(+)-thalassemia: Hb Zurich Albisrieden [alpha59(E8)Gly-->Arg (alpha2)].
Dutly F; Fehr J; Goede JS; Morf M; Troxler H; Frischknecht H
Hemoglobin; 2004; 28(4):347-51. PubMed ID: 15658192
[TBL] [Abstract][Full Text] [Related]
9. Unstable Hb Perth in a Taiwanese subject: a T-->C substitution at codon 32 of the beta-globin gene creates an MspI site.
Chang JG; Liu HC; Shih MC; Liu SC; Chan WL; Tsai FJ
Hemoglobin; 2002 Feb; 26(1):91-4. PubMed ID: 11939520
[No Abstract] [Full Text] [Related]
10. Hb Nunobiki or alpha 2 141 (HC3)Arg-->Cys beta 2 in a Belgian female results from a CGT-->TGT mutation in the alpha 2-globin gene.
Kazanetz EG; Leonova JY; Huisman TH; van der Dijs FP; Smit JW
Hemoglobin; 1996 Nov; 20(4):443-5. PubMed ID: 8936471
[No Abstract] [Full Text] [Related]
11. Hb G-Chinese: a G-->C substitution at codon 30 of the alpha2-globin gene creates a PstI cutting site.
Chang JG; Shih MC; Liu SC; Chen CM; Chan WL; Peng CT
Hemoglobin; 2002 Feb; 26(1):95-7. PubMed ID: 11939521
[No Abstract] [Full Text] [Related]
12. Association of Hb Hope [beta136(H14)Gly-->Asp] and Hb H disease.
Svasti S; Yodsowon B; Sriphanich R; Winichagoon P; Boonkhan P; Suwanban T; Sawangareetrakul P; Srisomsap C; Ketudat-Cairns JR; Svasti J; Fucharoen S
Hemoglobin; 2001 Nov; 25(4):429-35. PubMed ID: 11791878
[No Abstract] [Full Text] [Related]
13. A new beta chain variant, Hb Vienna or beta77(EF1)His-->Gln.
Hopmeier P; Plaseska-Karanfilska D; Efremov GD
Hemoglobin; 1998 Jul; 22(4):391-5. PubMed ID: 9730371
[No Abstract] [Full Text] [Related]
14. A new alpha chain hemoglobin variant: Hb Al-Hammadi Riyadh [alpha75(EF4)Asp-->Val (alpha2)].
Burnichon N; Lacan P; Becchi M; Zanella-Cleon I; Aubry M; Mowafy M; Couprie N; Francina A
Hemoglobin; 2006; 30(2):155-64. PubMed ID: 16798639
[TBL] [Abstract][Full Text] [Related]
15. The Hb Tarrant [alpha126(H9)Asp-->Asn]] mutation is localized in the alpha2-globin gene.
Perea FJ; Zamudio G; Meillon LA; Ibarra B
Hemoglobin; 1999 Aug; 23(3):295-7. PubMed ID: 10490145
[No Abstract] [Full Text] [Related]
16. Hb Bleuland [alpha108(G15)Thr-->Asn, ACC-->AAC (alpha2)]: a new abnormal hemoglobin associated with a mild alpha-thalassemia phenotype.
Harteveld CL; Versteegh FG; Kok PJ; van Rooijen-Nijdam IH; van Delft P; Giordano PC
Hemoglobin; 2006; 30(3):349-54. PubMed ID: 16840225
[TBL] [Abstract][Full Text] [Related]
17. Hb Marineo [beta70(E14)Ala-->Val]: a silent hemoglobin variant with a mutation within the heme pocket.
Giambona A; Vinciguerra M; Cassarà F; Li Muli R; Leto F; Passarello C; Wajcman H; Maggio A
Hemoglobin; 2006; 30(2):139-48. PubMed ID: 16798637
[TBL] [Abstract][Full Text] [Related]
18. Hb A2-Monreale [delta146(HC3)His-->Arg], a novel delta chain variant detected in west Sicily.
De Angioletti M; Di Girgenti C; Messineo R; Capra M; Carestia C
Hemoglobin; 2002 Feb; 26(1):1-5. PubMed ID: 11939506
[TBL] [Abstract][Full Text] [Related]
19. Hb Gerland [alpha55(E4)Val-->Ala (alpha2)]: a new neutral alpha chain variant involving the alpha2 gene.
Lacan P; Aubry M; Couprie N; Francina A
Hemoglobin; 2001 Nov; 25(4):417-20. PubMed ID: 11791875
[No Abstract] [Full Text] [Related]
20. A new beta-globin variant: Hb Sainte Eugénie [beta104(G6)Arg-->Trp] in a French Caucasian female.
Lacan P; Drai J; Aubry M; Francina A; Orgiazzi J
Hemoglobin; 2000 Aug; 24(3):245-8. PubMed ID: 10975444
[No Abstract] [Full Text] [Related]
[Next] [New Search]
