-
1
-
-
0021750055
-
Characterization of the human factor VIII gene
-
Gitschier J., Wood WI, Goralka TM, et al. Characterization of the human factor VIII gene. Nature. 1984 ; 312: 326-330.
-
(1984)
Nature
, vol.312
, pp. 326-330
-
-
Gitschier, J.1
Wood, W.I.2
Goralka, T.M.3
-
2
-
-
0027520025
-
Inversions disrupting the factor VIII gene are a common cause of severe haemophilia a
-
Lakich D., Kazazian HH Jr, Antonarakis SE, et al. Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A. Nat Genet. 1993 ; 5: 236-241.
-
(1993)
Nat Genet
, vol.5
, pp. 236-241
-
-
Lakich, D.1
Kazazian Jr., H.H.2
Antonarakis, S.E.3
-
3
-
-
0007416053
-
-
Census of India 2001. Available at: http://www.censusindia.net/results/ resultsmain.html.
-
Census of India 2001
-
-
-
4
-
-
0002511116
-
Inherited bleeding disorders
-
Oxford: Heinemann Medical Books;
-
Tuddenham EG Inherited bleeding disorders. In: Hoffbrand AV, Lewis SM, eds. Postgraduate Haematology. Oxford: Heinemann Medical Books ; 1989: 645.
-
Postgraduate Haematology
, vol.1989
, pp. 645
-
-
Tuddenham, E.G.1
-
5
-
-
23444434634
-
Factor VIII gene rearrangements in patients with severe haemophilia a
-
Goodeve AC, Preston FE, Peake IR Factor VIII gene rearrangements in patients with severe haemophilia A. Lancet. 1994 ; 343: 329-330.
-
(1994)
Lancet
, vol.343
, pp. 329-330
-
-
Goodeve, A.C.1
Preston, F.E.2
Peake, I.R.3
-
6
-
-
0029865410
-
Characterization of the Factor VIII defect in 147 patients with sporadic hemophilia A: Family studies indicate a mutation type-dependent sex ratio of mutation frequencies
-
Becker J., Schwaab R., Moller-Taube A., et al. Characterization of the Factor VIII defect in 147 patients with sporadic hemophilia A: family studies indicate a mutation type-dependent sex ratio of mutation frequencies. Am J Hum Genet. 1996 ; 58: 657-670.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 657-670
-
-
Becker, J.1
Schwaab, R.2
Moller-Taube, A.3
-
7
-
-
0027351077
-
Haemophilia: Strategies for carrier detection and prenatal diagnosis [review]
-
Peake IR, Lillicrap DP, Boulyjenkov V., et al. Haemophilia: strategies for carrier detection and prenatal diagnosis [review]. Bull World Health Organ. 1993 ; 71: 429-458.
-
(1993)
Bull World Health Organ
, vol.71
, pp. 429-458
-
-
Peake, I.R.1
Lillicrap, D.P.2
Boulyjenkov, V.3
-
8
-
-
1842353216
-
Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants
-
Kunkel LM, Smith KD, Boyer SH, et al. Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants. Proc Natl Acad Sci USA. 1977 ; 74: 1245-1249.
-
(1977)
Proc Natl Acad Sci USA
, vol.74
, pp. 1245-1249
-
-
Kunkel, L.M.1
Smith, K.D.2
Boyer, S.H.3
-
9
-
-
0023242425
-
An improved method of prenatal diagnosis of disease by analysis of amplified DNA sequences-application to haemophilia a
-
Kogan SC, Doherty M., Gitschier J. An improved method of prenatal diagnosis of disease by analysis of amplified DNA sequences-application to haemophilia A. N Engl J Med. 1987 ; 317: 985-990.
-
(1987)
N Engl J Med
, vol.317
, pp. 985-990
-
-
Kogan, S.C.1
Doherty, M.2
Gitschier, J.3
-
10
-
-
0025149521
-
The utility of a HindIII polymorphism of factor VIII examined by rapid DNA analysis
-
Graham JB, Kunkel GR, Fowlkes DM, et al. The utility of a HindIII polymorphism of factor VIII examined by rapid DNA analysis. Br J Haematol. 1990 ; 76: 75-79.
-
(1990)
Br J Haematol
, vol.76
, pp. 75-79
-
-
Graham, J.B.1
Kunkel, G.R.2
Fowlkes, D.M.3
-
11
-
-
0030934641
-
Factor VIII and IX gene polymorphisms and carrier analysis in Indian population
-
Shetty S., Ghosh K., Pathare A., et al. Factor VIII and IX gene polymorphisms and carrier analysis in Indian population. Am J Hematol. 1997 ; 54: 271-275.
-
(1997)
Am J Hematol
, vol.54
, pp. 271-275
-
-
Shetty, S.1
Ghosh, K.2
Pathare, A.3
-
12
-
-
0033670558
-
Factor VIII gene polymorphisms in the Asian Indian population
-
Chowdhury MR, Herrmann FH, Schroder W., et al. Factor VIII gene polymorphisms in the Asian Indian population. Hemophilia. 2000 ; 6: 625-630.
-
(2000)
Hemophilia
, vol.6
, pp. 625-630
-
-
Chowdhury, M.R.1
Herrmann, F.H.2
Schroder, W.3
-
13
-
-
0036844478
-
Factor VIII gene polymorphisms in north Indian population: A consensus algorithm for carrier analysis of hemophilia a
-
Srinivasan A., Mukhopadhyay S., Karim Z., et al. Factor VIII gene polymorphisms in north Indian population: a consensus algorithm for carrier analysis of hemophilia A. Clin Chim Acta. 2002 ; 325: 177-181.
-
(2002)
Clin Chim Acta
, vol.325
, pp. 177-181
-
-
Srinivasan, A.1
Mukhopadhyay, S.2
Karim, Z.3
-
14
-
-
0036834740
-
Carrier analysis and prenatal diagnosis of haemophilia a in North India
-
Pandey GS, Phadke SR, Mittal B. Carrier analysis and prenatal diagnosis of haemophilia A in North India. Int J Mol Med. 2002 ; 10: 661-664.
-
(2002)
Int J Mol Med
, vol.10
, pp. 661-664
-
-
Pandey, G.S.1
Phadke, S.R.2
Mittal, B.3
-
15
-
-
4844230309
-
Informative-ness of linkage analysis for genetic diagnosis of haemophilia a in India
-
Jayandharan G., Shaji RV, George B., et al. Informative-ness of linkage analysis for genetic diagnosis of haemophilia A in India. Haemophilia. 2004 ; 10: 553-559.
-
(2004)
Haemophilia
, vol.10
, pp. 553-559
-
-
Jayandharan, G.1
Shaji, R.V.2
George, B.3
-
16
-
-
0026535384
-
Registry of DNA polymorphisms within or close to the human factor VIII and factor IX genes. for the factor VIII/IX subcommittee of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis
-
Peake I. Registry of DNA polymorphisms within or close to the human factor VIII and factor IX genes. For the factor VIII/IX subcommittee of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost. 1992 ; 67: 227-280.
-
(1992)
Thromb Haemost
, vol.67
, pp. 227-280
-
-
Peake, I.1
-
17
-
-
0026089883
-
Restriction fragment length polymorphisms associated with the Factor VIII and Factor IX genes in Polynesians
-
Neil SV, Derry R., Paul AO Restriction fragment length polymorphisms associated with the Factor VIII and Factor IX genes in Polynesians. J Med Genet. 1991 ; 28: 171-176.
-
(1991)
J Med Genet
, vol.28
, pp. 171-176
-
-
Neil, S.V.1
Derry, R.2
Paul, A.O.3
-
18
-
-
0023794914
-
Carrier detection in 50 haemophilia a kindred by means of three intragenic and two extragenic restriction fragment length polymorphisms
-
Moodie P., Liddell MB, Peake IR, et al. Carrier detection in 50 haemophilia A kindred by means of three intragenic and two extragenic restriction fragment length polymorphisms. Br J Haematol. 1988 ; 70: 77-84.
-
(1988)
Br J Haematol
, vol.70
, pp. 77-84
-
-
Moodie, P.1
Liddell, M.B.2
Peake, I.R.3
-
19
-
-
0023235793
-
Haemophilia A: Carrier detection and prenatal diagnosis by linkage analysis using DNA polymorphism
-
Tuddenham EG, Goldman E., McGraw A., et al. Haemophilia A: carrier detection and prenatal diagnosis by linkage analysis using DNA polymorphism. J Clin Pathol. 1987 ; 40: 971-977.
-
(1987)
J Clin Pathol
, vol.40
, pp. 971-977
-
-
Tuddenham, E.G.1
Goldman, E.2
McGraw, A.3
-
20
-
-
0022253004
-
Hemophilia A. Detection of molecular defects and of carriers by DNA analysis
-
Antonarakis SE, Waber PG, Kittur SD, et al. Hemophilia A. Detection of molecular defects and of carriers by DNA analysis. N Engl J Med. 1985 ; 313: 842-848.
-
(1985)
N Engl J Med.
, vol.313
, pp. 842-848
-
-
Antonarakis, S.E.1
Waber, P.G.2
Kittur, S.D.3
-
21
-
-
0033932856
-
Experience of a single Italian center in genetic counseling for hemophilia: From linkage analysis to molecular diagnosis
-
Tagariello G., Belvini D., Salviato R., et al. Experience of a single Italian center in genetic counseling for hemophilia: from linkage analysis to molecular diagnosis. Haematologica. 2000 ; 85: 525-529.
-
(2000)
Haematologica
, vol.85
, pp. 525-529
-
-
Tagariello, G.1
Belvini, D.2
Salviato, R.3
-
22
-
-
0028168988
-
Allele frequencies and molecular diagnosis in hemophilia a and B patients from Russia and from some Asian Republics of the former U.S.S.R
-
Aseev M., Surin V., Baboev K., et al. Allele frequencies and molecular diagnosis in hemophilia A and B patients from Russia and from some Asian Republics of the former U.S.S.R. Prenat Diagn. 1994 ; 14: 513-522.
-
(1994)
Prenat Diagn
, vol.14
, pp. 513-522
-
-
Aseev, M.1
Surin, V.2
Baboev, K.3
-
23
-
-
0023714172
-
Restriction fragment length polymorphisms associated with factor VIII: C gene in Chinese
-
Chan V., Chan TK, Liu VW, et al. Restriction fragment length polymorphisms associated with factor VIII: C gene in Chinese. Hum Genet. 1988 ; 79: 128-131.
-
(1988)
Hum Genet
, vol.79
, pp. 128-131
-
-
Chan, V.1
Chan, T.K.2
Liu, V.W.3
-
24
-
-
0023713434
-
Carrier detection in Japanese hemophilia a by use of three intragenic and two extragenic factor VIII DNA probes: A study of 24 kindreds
-
Suehiro K., Tanimoto M., Hamaguchi M., et al. Carrier detection in Japanese hemophilia A by use of three intragenic and two extragenic factor VIII DNA probes: a study of 24 kindreds. J Lab Clin Med. 1988 ; 112: 314-318.
-
(1988)
J Lab Clin Med
, vol.112
, pp. 314-318
-
-
Suehiro, K.1
Tanimoto, M.2
Hamaguchi, M.3
-
25
-
-
0036474477
-
Suitability of four polymorphic DNA makers for indirect genetic diagnosis of hemophilia a in Japanese subjects
-
Sawada A., Sumita C., Higasa S., et al. Suitability of four polymorphic DNA makers for indirect genetic diagnosis of hemophilia A in Japanese subjects. Thromb Res. 2002 ; 105: 271-276.
-
(2002)
Thromb Res
, vol.105
, pp. 271-276
-
-
Sawada, A.1
Sumita, C.2
Higasa, S.3
-
26
-
-
0027653964
-
The prevalence study on restriction fragment length polymorphism analysis for the detection of hemophilia a carrier
-
Song KS, Lee CH, Chung CS, et al. The prevalence study on restriction fragment length polymorphism analysis for the detection of hemophilia A carrier. Yonsei Med J. 1993 ; 34: 239-242.
-
(1993)
Yonsei Med J
, vol.34
, pp. 239-242
-
-
Song, K.S.1
Lee, C.H.2
Chung, C.S.3
-
27
-
-
0028289158
-
A comparison of the allelic frequencies of ten DNA polymorphisms associated with factor VIII and factor IX genes in Thai and western
-
Goodeve AC, Chuansumrit A., Sasanakul W., et al. A comparison of the allelic frequencies of ten DNA polymorphisms associated with factor VIII and factor IX genes in Thai and western European populations. Blood Coagul Fibrinolysis. 1994 ; 5: 29-35.
-
(1994)
European Populations. Blood Coagul Fibrinolysis
, vol.5
, pp. 29-35
-
-
Goodeve, A.C.1
Chuansumrit, A.2
Sasanakul, W.3
-
28
-
-
0035011652
-
Factor VIII gene inversions and polymorphisms in Brazilian patients with haemophilia A: Carrier detection and prenatal diagnosis
-
Soares RP, Chamone DA, Bydlowski SP Factor VIII gene inversions and polymorphisms in Brazilian patients with haemophilia A: carrier detection and prenatal diagnosis. Haemophilia. 2001 ; 7: 299-305.
-
(2001)
Haemophilia
, vol.7
, pp. 299-305
-
-
Soares, R.P.1
Chamone, D.A.2
Bydlowski, S.P.3
-
29
-
-
0025349370
-
Investigation of factor VIII: C gene restriction fragment length polymorphisms and search for deletion in hemophiliac subjects in Algeria
-
Nafa K., Meriane F., Reghis A., et al. Investigation of factor VIII: C gene restriction fragment length polymorphisms and search for deletion in hemophiliac subjects in Algeria. Hum Genet. 1990 ; 84: 401-405.
-
(1990)
Hum Genet
, vol.84
, pp. 401-405
-
-
Nafa, K.1
Meriane, F.2
Reghis, A.3
|