166 related articles for article (PubMed ID: 16840232)
1. Molecular diagnosis of a case of Hb Phnom Penh [alpha117(GH5)Phe-I1e-alpha118(H1)Thr (alpha1)].
Leung RY; Ma ES; Chan AY; Chow EY
Hemoglobin; 2006; 30(3):397-9. PubMed ID: 16840232
[TBL] [Abstract][Full Text] [Related]
2. Association of Hb Thailand [α56(E5)Lys→Thr] and Hb Phnom Penh [α117(GH5)-Ile-α118(H1)] with α(0)-thalassemia: molecular and hematological features and differential diagnosis.
Singha K; Srivorakun H; Fucharoen G; Changtrakul Y; Komwilaisak P; Jetsrisuparb A; Puangplruk R; Fucharoen S
Hemoglobin; 2013; 37(1):37-47. PubMed ID: 23215800
[TBL] [Abstract][Full Text] [Related]
3. A novel case of Hb Phnom Penh: codons 117/118 (+ATC) as a cause of α+ -thalassemia.
Zhai YS; Tang HS; Zhou JY; Li DZ
Hemoglobin; 2012; 36(3):289-92. PubMed ID: 22432594
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Hb A2-Pasteur-Tunis [delta59(E3)Lys-->Asn, AAG-->AAC]: a new delta chain variant detected by DNA sequencing in a Tunisian carrier of the codon 39 (C-->T) beta0-Thalassemia mutation.
Moumni I; Zorai A; Daoued BB; Mosbahi I; Omar S; Kaabachi N; Dellagi K; Abbes S
Hemoglobin; 2007; 31(1):23-9. PubMed ID: 17365002
[TBL] [Abstract][Full Text] [Related]
6. Molecular lesion frequency of hemoglobin gene disorders in Taiwan.
Liu SC; Peng CT; Lin TH; Wang SJ; Shih MC; Tien N; Chang CC; Lu JJ; Lin CY
Hemoglobin; 2011; 35(3):228-36. PubMed ID: 21599435
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Hb Barika [alpha42(C7)Tyr-->His (alpha2)] leads to an alpha+ -Thalassemia-like syndrome.
Préhu C; Riou J; Wajcman H
Hemoglobin; 2007; 31(1):17-22. PubMed ID: 17365001
[TBL] [Abstract][Full Text] [Related]
9. Utilization of different methodologies for the characterization of Hb Hasharon heterozygotes.
Chinelato-Fernandes AR; Mendiburu CF; Bonini-Domingos CR
Genet Mol Res; 2006 Mar; 5(1):1-6. PubMed ID: 16755491
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. Hemoglobin Loves Park [beta68 (E12) Leu-->Phe]: report of five cases including one originating from a de novo mutation.
Ferreira C; Hoyer JD; Miranda A; Picanço I; Almendra V; Seixas MT; Almeida T; Romão L; Faustino P
Am J Hematol; 2006 Apr; 81(4):256-61. PubMed ID: 16550507
[TBL] [Abstract][Full Text] [Related]
13. Hb Southampton [beta106(G8)Leu-->Pro, CTG-->CCG] in an Argentinean boy.
Eandi Eberle S; Noguera NI; Sciuccati G; Bonduel M; Díaz L; Staciuk R; Feliu-Torres A
Hemoglobin; 2006; 30(3):401-3. PubMed ID: 16840233
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. A new electrophoretically silent beta-globin variant in a Portuguese family: Hb Viseu [beta57(E1)Asn --> Thr].
Frischknecht H; Troxler H; Forster C; Dutly F
Hemoglobin; 2006; 30(1):23-7. PubMed ID: 16540411
[TBL] [Abstract][Full Text] [Related]
16. Hb La Coruña [beta38(C4)Thr-->Ile]: a new hemoglobin variant leading to familial polycythemia.
Ropero P; Fernández-Lago C; Villegas A; Polo M; Mateo M; Mora A; González FA
Hemoglobin; 2006; 30(3):379-83. PubMed ID: 16840229
[TBL] [Abstract][Full Text] [Related]
17. Hemoglobin Phnom Penh [alpha117Phe(H1)-Ile-alpha118Thr(H2)]; evidence for a hotspot for insertion of residues in the third exon of the alpha1-globin gene.
Wajcman H; Préhu MO; Préhu C; Blouquit Y; Promé D; Galactéros F
Hum Mutat; 1998; Suppl 1():S20-2. PubMed ID: 9452028
[No Abstract] [Full Text] [Related]
18. Two new mutations in cis on (G)gamma chain of fetal hemoglobin: Hb F-Madrid [G gamma 50(D1)Ser-->Cys] and [G gamma 75(E19)Ile-->Thr].
Hojas R; Villegas A; Ropero P; Valverde F; Nogales A; González FA; José C; Villar L; García C
Ann Hematol; 2003 Mar; 82(3):181-3. PubMed ID: 12634953
[TBL] [Abstract][Full Text] [Related]
19. High oxygen affinity hemoglobin variant in a Canadian family: Hb Bunbury [beta94(FG1)Asp-->Asn, GAC-->AAC].
Walker L; Eng B; McFarlane A; Waye JS
Hemoglobin; 2007; 31(1):101-3. PubMed ID: 17365011
[TBL] [Abstract][Full Text] [Related]
20. Hemoglobin I-Philadelphia [alpha 16 (A14) LYS-->GLU] heterozygote among blood donors from Brazil.
Torres FR; Ondei LS; Zamaro PJ; Silva RU; Cavasini CE; Rossit AR; Machado RL; Bonini-Domingos CR
Genet Mol Res; 2006 Dec; 5(4):713-6. PubMed ID: 17183481
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
