These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

122 related articles for article (PubMed ID: 16156020)

  • 1. Gene symbol: HBA1. Disease: Haemoglobin alpha 1.
    Vazão H; Bento C; Ribeiro L
    Hum Genet; 2005 Jul; 117(2-3):296. PubMed ID: 16156020
    [No Abstract]   [Full Text] [Related]  

  • 2. Hb G-Waimanalo [A1] [α64(E13)Asp→Asn; HBA1: c.193 G > A] with Decreased Oxygen Affinity.
    Karow A; Eekels JJ; Zurbriggen K; Schmid M; Schmugge M; Speer O
    Hemoglobin; 2015; 39(6):432-4. PubMed ID: 26291968
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Diagnosis and molecular characterization of a novel α
    Makis A; Georgiou I; Traeger-Synodinos J; Chaliasos N; Grosso M; Gambale A; Iolascon A
    Int J Lab Hematol; 2017 Oct; 39(5):e124-e126. PubMed ID: 28603861
    [No Abstract]   [Full Text] [Related]  

  • 4. Homozygosity for HBA1: c.179G > A: Hb Adana in an infant.
    Aksu T; Yarali N; Bayram C; Fettah A; Avci Z; Tunç B
    Hemoglobin; 2014; 38(6):449-50. PubMed ID: 25342395
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hb G-Waimanalo [A1] or α64(E13)Asp→Asn (α1) (HBA1: c.193G>A) Observed in a Bulgarian Family.
    Petkov G; Dimishkovska M; Tsoneva Ivanova V; Yordanov G; Zdraveski A; Plaseska-Karanfilska D
    Hemoglobin; 2015; 39(6):430-1. PubMed ID: 26212674
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular analysis of complex cases of alpha- and beta-thalassemia in Mexican mestizo patients with microcytosis and hypochromia reveals two novel alpha(0) -thalassemia deletions - -(Mex1) and - -(Mex2).
    de-la-Cruz-Salcedo EI; Ibarra B; Rizo-de-la-Torre LC; Sánchez-López JY; González-Mercado A; Harteveld CL; Perea-Díaz FJ
    Int J Lab Hematol; 2016 Oct; 38(5):535-42. PubMed ID: 27339814
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of a new HBA1 gene mutation (HBA1:c.301-2A>T) in cis with Hb Riccarton (HBA1:c.154G>A) [α51(CE9)Gly→Ser].
    Scheps KG; Binaghi A; Varela V
    Hemoglobin; 2012; 36(5):504-7. PubMed ID: 22738642
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hb Jishui [
    Xie W; Zheng H; Xu A; Ji L
    Hemoglobin; 2021 Jul; 45(4):259-261. PubMed ID: 34802367
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Evidence for a gene conversion in a Hb Arya Carrier [α codon 47 Asp>Asn, Hb A1(or Hb A2):c.142 G>A].
    Pécriaux A; Paillard C; Galoisy A; Riou J; Le Metayer N; Wajcman H; Pissard S
    Int J Lab Hematol; 2017 Jun; 39(3):e55-e59. PubMed ID: 28042694
    [No Abstract]   [Full Text] [Related]  

  • 10. [Hemoglobin Köln disease: familial hypochromic hemolytic anemia with hemoglobin anomaly].
    Pribilla W; Klesse P; Betke K; Lehmann H; Beale D
    Klin Wochenschr; 1965 Oct; 43(19):1049-53. PubMed ID: 5881530
    [No Abstract]   [Full Text] [Related]  

  • 11. Novel human pathological mutations. Gene symbol: HBA1. Disease: haemoglobin variant.
    Refaldi C; Gensini F; Cappellini MD
    Hum Genet; 2009 Aug; 126(2):343. PubMed ID: 19694032
    [No Abstract]   [Full Text] [Related]  

  • 12. Hb Capa or alpha (2)94(G1)Asp-->Gly beta 2, a mildly unstable variant with an A-->G (GAC-->GGC) mutation in codon 94 of the alpha 1-globin gene.
    Dinçol G; Dinçol K; Erdem S; Pobedimskaya DD; Molchanova TP; Ye Z; Webber BB; Wilson JB; Huisman TH
    Hemoglobin; 1994 Jan; 18(1):57-60. PubMed ID: 8195009
    [No Abstract]   [Full Text] [Related]  

  • 13. Two new hemoglobin variants: Hb Brem-sur-Mer [beta9(A6)Ser-->Tyr] and Hb Passy [alpha81(F2)Ser-->Pro (alpha2)].
    Lacan P; Moreau M; Becchi M; Zanella-Cleon I; Aubry M; Louis JJ; Couprie N; Francina A
    Hemoglobin; 2005; 29(1):69-75. PubMed ID: 15768558
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of Mutations Causing Aberrant Termination and Deficient Splice Donor Site on the HBA1 Gene.
    Farashi S; Vakili S; Garous NF; Ashki M; Forouzesh Pour F; Zeinali F; Rad F; Imanian H; Azarkeivan A; Najmabadi H
    Hemoglobin; 2016; 40(1):38-43. PubMed ID: 26531168
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Hemoglobin D Punjab in Dagestan].
    Khasaev ASh; Shamov IA; Kulagin MN; Kolodeĭ SV; Spivak VA
    Gematol Transfuziol; 1983 Jun; 28(6):47-8. PubMed ID: 6884742
    [No Abstract]   [Full Text] [Related]  

  • 16. Compound heterozygosity for Hb Spanish town [alpha27(B8)Glu-->Val], Hb S [beta6(A3)Glu-->Val] and the -alpha(3.7kb) thalassemia deletion.
    Faustino P; Picanço I; Miranda A; Seixas T; Ferrão A; Morais A; Lavinha J; Romão L
    Hemoglobin; 2002 May; 26(2):185-9. PubMed ID: 12144063
    [No Abstract]   [Full Text] [Related]  

  • 17. Hb Fulton-Georgia [α20(B1)His→Pro; HBA1: c.62A>C]: a new α-globin variant coinherited with α-thalassemia-2 (3.7 kb deletion) and Hb SC disease.
    Zhuang L; Patel N; Bryant S; Kutlar A; Kutlar F; Young AN
    Hemoglobin; 2013; 37(5):481-5. PubMed ID: 24006930
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hb Milano [α109(G16)Leu→Pro (C
    Curcio C; Giannone V; Benzoni E; Cesaretti C; Ivaldi G
    Hemoglobin; 2019 Jan; 43(1):4-6. PubMed ID: 31084368
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Two α1-Globin Gene Point Mutations Causing Severe Hb H Disease.
    Jiang H; Huang LY; Zhen L; Jiang F; Li DZ
    Hemoglobin; 2017; 41(4-6):293-296. PubMed ID: 29115167
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [The second family with hemoglobin Dagestan (alpha 60 Lys----Glu)].
    Khasaev ASh; Shamov IA; Aseeva EA; Spivak VA
    Gematol Transfuziol; 1990 Mar; 35(3):6-8. PubMed ID: 2361588
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.