153 related articles for article (PubMed ID: 31973650)
1. An Unusual Compound Heterozygosity for Hb O-Arab (
van Gammeren AJ; Pelkmans L; Endschot CCWV; Roelofsen-de Beer RJAC; Harteveld CL
Hemoglobin; 2020 Jan; 44(1):61-63. PubMed ID: 31973650
[TBL] [Abstract][Full Text] [Related]
2. Hb Rush (
Mashon RS; Das R; Dhawan R; Kakkar N; Dhar T
Hemoglobin; 2020 Jan; 44(1):64-66. PubMed ID: 32124638
[TBL] [Abstract][Full Text] [Related]
3. Hb Matera (HBB: c.167 T > A): A Second Case Detected in a Pregnant Chinese Woman by the Capillary Electrophoresis Method.
Li YQ; Ye LH; Mo Y
Hemoglobin; 2016; 40(2):125-6. PubMed ID: 26911301
[TBL] [Abstract][Full Text] [Related]
4. Association between Different Polymorphic Markers and β-Thalassemia Intermedia in Central Iran.
Sajadpour Z; Amini-Farsani Z; Motovali-Bashi M; Yadollahi M; Khosravi-Farsani N
Hemoglobin; 2020 Jan; 44(1):27-30. PubMed ID: 31899996
[TBL] [Abstract][Full Text] [Related]
5. Hb Knossos (HBB: c.82G > T), β-globin CD 5 (-CT) (HBB: c.17_18delCT) and δ-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia.
Moassas F; Nweder MS; Murad H
BMC Pediatr; 2019 Feb; 19(1):61. PubMed ID: 30777047
[TBL] [Abstract][Full Text] [Related]
6. Compound Heterozygosity for Hb Alperton (HBB: c.407C>T) and IVS-I-5 (G>C) (HBB: c.92+5G>C) Mutations Presenting as a Moderate Anemia in an Indian Family.
Godbole KG; Ramachandran A; Karkamkar AS; Dalal AB
Hemoglobin; 2018 Mar; 42(2):141-142. PubMed ID: 29651865
[TBL] [Abstract][Full Text] [Related]
7. Mild Microcytic Anemia in an Infant with a Compound Heterozygosity for Hb C (HBB: c.19G > A) and Hb Osu Christiansborg (HBB: c.157G > A).
Boucher MO; Chui DH; Woda BA; Newburger PE
Hemoglobin; 2016 Jun; 40(3):208-9. PubMed ID: 27117572
[TBL] [Abstract][Full Text] [Related]
8. Coinheritance of Hb D-Punjab and β-thalassemia: diagnosis and implications in prenatal diagnosis.
Das S; Mashon RS
Hemoglobin; 2015; 39(2):138-40. PubMed ID: 25666204
[TBL] [Abstract][Full Text] [Related]
9. First Report of a Coincidental Discovery of Hb Antibes-Juan-Les-Pins (
Theodoridou S; Boutou E; Vyzantiadis TA; Balassopoulou A; Vlachaki E
Hemoglobin; 2020 Sep; 44(5):361-363. PubMed ID: 33267629
[TBL] [Abstract][Full Text] [Related]
10. A Novel β-Thalassemia Mutation [IVS-I-6 (T>G),
Luo H; Zou Y; Liu Y
Hemoglobin; 2020 Jan; 44(1):55-57. PubMed ID: 31939318
[TBL] [Abstract][Full Text] [Related]
11. Hb S (
Azarkeivan A; Cohan N; Niazkar HR; Azizi A; Rad F
Hemoglobin; 2020 Mar; 44(2):109-112. PubMed ID: 32370567
[TBL] [Abstract][Full Text] [Related]
12. A Case Report of Compound Heterozygosity for β
Intasai N; Phasit A; Panyasai S; Pornprasert S
Hemoglobin; 2019 Jan; 43(1):63-65. PubMed ID: 31037981
[TBL] [Abstract][Full Text] [Related]
13. Missing Hb Q-India Peak in a Triple-Heterozygous Patient with Hb D-Punjab/Hb Q-India/β-Thalassemia Trait.
Sharma P; Jandial A; Rajasekaran S; Das R; Chhabra S; Hira JK; Khadwal AR; Malhotra P; Sharma P
Hemoglobin; 2020 May; 44(3):211-213. PubMed ID: 32448026
[TBL] [Abstract][Full Text] [Related]
14. Compound Heterozygosity for Hb D-Ibadan (HBB: c.263C>A) and Hb C (HBB: c.19G>A).
Kundrapu S; Janaki N; Meyerson HJ
Hemoglobin; 2018 Jul; 42(4):269-271. PubMed ID: 30604644
[TBL] [Abstract][Full Text] [Related]
15. Rare Association of Hb D-Los Angeles (HBB: c.364G>C) with Hb H Disease: Diagnosis and Clinical Implications.
Zioga A; Thanopoulou E; Hatzi E; Chaliasos N; Georgiou I; Makis A
Hemoglobin; 2018; 42(5-6):336-338. PubMed ID: 30626242
[TBL] [Abstract][Full Text] [Related]
16. Hb Midnapore [β53(D4)Ala→Val; HBB: c.161C>T]: A Novel Hemoglobin Variant with a Structural Abnormality Associated with IVS-I-5 (G>C) (HBB: c.92+5G>C) Found in a Bengali Indian Family.
Panja A; Chowdhury P; Basu A
Hemoglobin; 2016 Sep; 40(5):300-303. PubMed ID: 27690257
[TBL] [Abstract][Full Text] [Related]
17. A Clinical Update of the Hb Siirt [β27(B9)Ala→Gly; HBB: c.83C>G] Hemoglobin Variant.
Cappabianca MP; Colosimo A; Sabatucci A; Dainese E; Di Biagio P; Piscitelli R; Sarra O; Zei D; Amato A
Hemoglobin; 2017 Jan; 41(1):53-55. PubMed ID: 28391745
[TBL] [Abstract][Full Text] [Related]
18. Elevated Hb A₂ Levels in a Patient with a Compound Heterozygosity for the (β⁺) -31 (A > G) and (β⁰) Codon 17 (A > T) Mutations Together with a Single α-Globin Gene.
Panyasai S; Jaiping K; Pornprasert S
Hemoglobin; 2015; 39(4):292-5. PubMed ID: 26029792
[TBL] [Abstract][Full Text] [Related]
19. First Detection of Hb Cenxi [β46(CD5)Gly→Arg (
Li YQ; Li YW; Liang L; Meng MH; Zhang XQ
Hemoglobin; 2021 Jul; 45(4):262-264. PubMed ID: 31985312
[TBL] [Abstract][Full Text] [Related]
20. Compound Heterozygote for a Novel Elongated C-Terminal β-Globin Variant (
Nuinoon M; Thipthara O; Fucharoen S
Hemoglobin; 2019 Jan; 43(1):52-55. PubMed ID: 31106603
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]