178 related articles for article (PubMed ID: 22221849)
1. Heterozygote frequencies of common polymorphic markers of factor VIII (f8) and factor IX (f9) genes in indigenous Nepali population.
Kanani P; Poudyal BS; Shetty S; Kapali SM; Ghosh K
Haemophilia; 2012 Mar; 18(2):e44-5. PubMed ID: 22221849
[No Abstract] [Full Text] [Related]
2. Molecular biology of the hemophilias.
Thompson AR
Prog Hemost Thromb; 1991; 10():175-214. PubMed ID: 1901173
[No Abstract] [Full Text] [Related]
3. Factor VIII and IX genes polymorphisms in a Brazilian black population.
Arruda VR; Annichino-Bizzachi JM; Sonati Mde F; Costa FF
Thromb Haemost; 1993 Aug; 70(2):371. PubMed ID: 7901921
[No Abstract] [Full Text] [Related]
4. Common intragenic and extragenic polymorphisms of blood coagulation factors VIII and IX are different in Chinese and Caucasian populations.
de la Salle C; Wu Q; Baas MJ; Hanauer A; Ruan C; Cazenave JP
Clin Genet; 1990 Dec; 38(6):434-40. PubMed ID: 1981181
[TBL] [Abstract][Full Text] [Related]
5. Novel F8 and F9 gene variants from the PedNet hemophilia registry classified according to ACMG/AMP guidelines.
Andersson NG; Labarque V; Letelier A; Mancuso ME; Bührlen M; Fischer K; Kartal-Kaess M; Koskenvuo M; Mikkelsen T; Ljung R;
Hum Mutat; 2020 Dec; 41(12):2058-2072. PubMed ID: 32935414
[TBL] [Abstract][Full Text] [Related]
6. Reliable and cost-effective approach for diagnosis of heterozygous F8/F9 large deletions by quantitative real-time PCR.
Abelleyro MM; Radic CP; Tetzlaff T; Marchione V; Fundia AF; Larripa IB; Rossetti LC; De Brasi CD
Haemophilia; 2015 May; 21(3):e247-e251. PubMed ID: 25753911
[No Abstract] [Full Text] [Related]
7. Factor VIII and IX gene polymorphisms and carrier analysis in Indian population.
Shetty S; Ghosh K; Pathare A; Colah R; Badakare S; Mohanty D
Am J Hematol; 1997 Apr; 54(4):271-5. PubMed ID: 9092680
[TBL] [Abstract][Full Text] [Related]
8. [Population and molecular-genetic aspects of hemophilia A and B in Uzbekistan].
Boboev KT
Tsitol Genet; 2008; 42(2):51-4. PubMed ID: 18630121
[TBL] [Abstract][Full Text] [Related]
9. Recurrent F8 and F9 gene variants result from a founder effect in two large French haemophilia cohorts.
Lassalle F; Marmontel O; Zawadzki C; Fretigny M; Bouvagnet P; Vinciguerra C
Haemophilia; 2018 Jul; 24(4):e213-e221. PubMed ID: 29656491
[TBL] [Abstract][Full Text] [Related]
10. Application of a molecular diagnostic algorithm for haemophilia A and B using next-generation sequencing of entire F8, F9 and VWF genes.
Bastida JM; González-Porras JR; Jiménez C; Benito R; Ordoñez GR; Álvarez-Román MT; Fontecha ME; Janusz K; Castillo D; Fisac RM; García-Frade LJ; Aguilar C; Martínez MP; Bermejo N; Herrero S; Balanzategui A; Martin-Antorán JM; Ramos R; Cebeiro MJ; Pardal E; Aguilera C; Pérez-Gutierrez B; Prieto M; Riesco S; Mendoza MC; Benito A; Hortal Benito-Sendin A; Jiménez-Yuste V; Hernández-Rivas JM; García-Sanz R; González-Díaz M; Sarasquete ME
Thromb Haemost; 2017 Jan; 117(1):66-74. PubMed ID: 27734074
[TBL] [Abstract][Full Text] [Related]
11. [Structure and function of factor VIII and factor IX gene and molecular DNA diagnosis in hemophilia A and B].
Herrmann FH; Wehnert M; Wulff K
Z Arztl Fortbild (Jena); 1988; 82(22):1116-22. PubMed ID: 2907834
[No Abstract] [Full Text] [Related]
12. Restriction fragment length polymorphisms associated with the factor VIII and factor IX genes in Polynesians.
Van-de-Water NS; Ridgway D; Ockelford PA
J Med Genet; 1991 Mar; 28(3):171-6. PubMed ID: 1675686
[TBL] [Abstract][Full Text] [Related]
13. Factor levels in carriers of haemophilia are associated with familial severity: a Danish single centre study.
Funding E; Christiansen K; Poulsen LH
Haemophilia; 2015 Sep; 21(5):e440-2. PubMed ID: 26178416
[No Abstract] [Full Text] [Related]
14. The molecular genetics of hemophilia A and B in man. Factor VIII and factor IX deficiency.
Antonarakis SE
Adv Hum Genet; 1988; 17():27-59. PubMed ID: 3142226
[No Abstract] [Full Text] [Related]
15. [Genetic factors in hemophilia].
Rozynkowa D
Acta Haematol Pol; 1987; 18(1-2):96-100. PubMed ID: 3124485
[No Abstract] [Full Text] [Related]
16. Molecular basis of hemophilia.
Lozier JN; High KA
Hematol Pathol; 1990; 4(1):1-26. PubMed ID: 2111315
[No Abstract] [Full Text] [Related]
17. Single-tube tetradecaplex panel of highly polymorphic microsatellite markers < 1 Mb from F8 for simplified preimplantation genetic diagnosis of hemophilia A.
Zhao M; Chen M; Tan ASC; Cheah FSH; Mathew J; Wong PC; Chong SS
J Thromb Haemost; 2017 Jul; 15(7):1473-1483. PubMed ID: 28345288
[TBL] [Abstract][Full Text] [Related]
18. [Gene mutation and gene diagnosis of hemophilia].
Kojima T
Nihon Seirigaku Zasshi; 1998; 60(1):31-42. PubMed ID: 9614303
[No Abstract] [Full Text] [Related]
19. The Canadian "National Program for hemophilia mutation testing" database: a ten-year review.
Rydz N; Leggo J; Tinlin S; James P; Lillicrap D
Am J Hematol; 2013 Dec; 88(12):1030-4. PubMed ID: 23913812
[TBL] [Abstract][Full Text] [Related]
20. F8 and F9 mutations fail to co-segregate in a family with co-incident haemophilia A and B.
Siddiq S; Morse C; Goodeve A; Panayi M; Tait RC; Mumford A
Haemophilia; 2011 Jan; 17(1):e230-4. PubMed ID: 20860608
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]