310 related articles for article (PubMed ID: 2567219)
1. Partial deletions of factor VIII gene as molecular diagnostic markers in haemophilia A.
Wehnert M; Herrmann FH; Wulff K
Dis Markers; 1989; 7(2):113-7. PubMed ID: 2567219
[TBL] [Abstract][Full Text] [Related]
2. Carrier detection and prenatal diagnosis in families with haemophilia.
Shetty S; Ghosh K; Bhide A; Mohanty D
Natl Med J India; 2001; 14(2):81-3. PubMed ID: 11396323
[TBL] [Abstract][Full Text] [Related]
3. Genomic diagnosis of haemophilia A and B in the German Democratic Republic.
Herrmann FH; Wehnert M; Schröder W
Folia Haematol Int Mag Klin Morphol Blutforsch; 1990; 117(4):601-7. PubMed ID: 1714866
[TBL] [Abstract][Full Text] [Related]
4. Carrier detection and prenatal diagnosis in haemophilia A and B.
Chistolini A; Papacchini M; Mazzucconi MG; La Verde G; Arcieri R; Ferrari A; Paesano R; Pachi A; Mariani G
Haematologica; 1990; 75(5):424-8. PubMed ID: 1982946
[TBL] [Abstract][Full Text] [Related]
5. Carrier analysis and prenatal diagnosis of haemophilia A in North India.
Pandey GS; Phadke SR; Mittal B
Int J Mol Med; 2002 Nov; 10(5):661-4. PubMed ID: 12373312
[TBL] [Abstract][Full Text] [Related]
6. Identification of new dinucleotide-repeat polymorphisms in factor VIII gene using fluorescent PCR.
Kim JW; Park SY; Kim YM; Kim JM; Kim DJ; Ryu HM
Haemophilia; 2005 Jan; 11(1):38-42. PubMed ID: 15660987
[TBL] [Abstract][Full Text] [Related]
7. Informativeness of linkage analysis for genetic diagnosis of haemophilia A in India.
Jayandharan G; Shaji RV; George B; Chandy M; Srivastava A
Haemophilia; 2004 Sep; 10(5):553-9. PubMed ID: 15357783
[TBL] [Abstract][Full Text] [Related]
8. The use of DNA markers for carrier detection and prenatal diagnosis of haemophilia A in Egyptian families.
Hussein IR; El-Beshlawy A; Salem A; Mosaad R; Zaghloul N; Ragab L; Fayek H; Gaber K; El-Ekiabi M
Haemophilia; 2008 Sep; 14(5):1082-7. PubMed ID: 18547262
[TBL] [Abstract][Full Text] [Related]
9. Molecular genetics and counselling in haemophilia.
Peake I
Thromb Haemost; 1995 Jul; 74(1):40-4. PubMed ID: 8578494
[TBL] [Abstract][Full Text] [Related]
10. DNA analysis of haemophilia A families from southern France. Experience of a hospital laboratory.
Aguilar-Martinez P; Fabre N; Navarro R; Schved JF; Gris JC; Romey MC; Demaille J; Claustres M
Genet Couns; 1993; 4(4):311-9. PubMed ID: 7906519
[TBL] [Abstract][Full Text] [Related]
11. Hemophilia A. Detection of molecular defects and of carriers by DNA analysis.
Antonarakis SE; Waber PG; Kittur SD; Patel AS; Kazazian HH; Mellis MA; Counts RB; Stamatoyannopoulos G; Bowie EJ; Fass DN
N Engl J Med; 1985 Oct; 313(14):842-8. PubMed ID: 2993888
[TBL] [Abstract][Full Text] [Related]
12. A somatic mosaic for haemophilia A detected at the DNA level.
Higuchi M; Kochhan L; Olek K
Mol Biol Med; 1988 Feb; 5(1):23-7. PubMed ID: 3131627
[TBL] [Abstract][Full Text] [Related]
13. Application of intron 9 and intron 25 dinucleotide repeats of the factor VIII gene for carrier diagnosis in haemophilia A.
Venceslá A; Baena M; Fares Taie L; Cornet M; Baiget M; Tizzano EF
Haemophilia; 2008 May; 14(3):489-93. PubMed ID: 18384354
[TBL] [Abstract][Full Text] [Related]
14. Genotype assignment of haemophilia A by use of intragenic and extragenic restriction fragment length polymorphisms.
Bröcker-Vriends AH; Briët E; Quadt R; Dreesen JC; Bakker E; Claassen-Tegelaar R; Kanhai HH; van de Kamp JJ; Pearson PL
Thromb Haemost; 1987 Apr; 57(2):131-6. PubMed ID: 2885943
[TBL] [Abstract][Full Text] [Related]
15. Carrier detection and prenatal diagnosis of hemophilia A in a Korean population by PCR-based analysis of the BclI/intron 18 and St14 VNTR polymorphisms.
Choi YM; Hwang D; Choe J; Jun JK; Kim EJ; Moon SY; Cho S
J Hum Genet; 2000; 45(4):218-23. PubMed ID: 10944851
[TBL] [Abstract][Full Text] [Related]
16. Genomic carrier detection and prenatal diagnosis of haemophilia A in families at risk using the polymerase chain reaction (PCR).
Wehnert M; Shukova EL; Surin VL; Schröder W; Solovjev GYa ; Grinjeva NI; Herrmann FH
Folia Haematol Int Mag Klin Morphol Blutforsch; 1990; 117(4):617-22. PubMed ID: 1714868
[TBL] [Abstract][Full Text] [Related]
17. Factor VIII gene haplotypes and linkage disequilibrium for the indirect genetic analysis of hemophilia A in India.
Singh M; Singh P
Clin Appl Thromb Hemost; 2009; 15(3):334-9. PubMed ID: 18160577
[TBL] [Abstract][Full Text] [Related]
18. Gene analysis in haemophilia A--restriction fragment length polymorphism and molecular defects in the factor VIII gene.
Mikami S
Nihon Ketsueki Gakkai Zasshi; 1988 Dec; 51(8):1680-8. PubMed ID: 2907841
[No Abstract] [Full Text] [Related]
19. Carrier detection in Japanese haemophilia A families using factor VIII gene probe (F8A) and the gene-linked ST 14-1 probe.
Nishino M; Nishimura T; Naka H; Mikami S; Tokino T; Murotsu T
Jinrui Idengaku Zasshi; 1987 Sep; 32(3):237-45. PubMed ID: 3129604
[No Abstract] [Full Text] [Related]
20. [Diagnosis of hemophilia A by a combination of St14(DXS52) VNTR polymorphism and (CA)n repeat polymorphism within FVIII gene].
Zhong CG; Li LY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):80-2. PubMed ID: 14767918
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]