E-LIB Suche - Ergebnisse für: JAYANDHARAN, G. R.

1

Molecular basis of quantitative fibrinogen disorders in 27 ..:

Sumitha, E. ; Jayandharan, G. R. ; Arora, N....
Haemophilia. 19 (2013) 4 - p. 611-618 , 2013

Link: https://doi.org/10.1111/..

2

Fluorescent PCR-based gene dose analysis for detection of d..:

Devi, G. Sankari ; Arora, N. ; Rajkumar, S. V....
Haemophilia. 19 (2013) 6 - p. e377-e380 , 2013

Link: https://doi.org/10.1111/..

3

Nuclear factor (NF)-κB and its associated pathways are majo..:

Sen, D. ; Chapla, A. ; Walter, N....
Journal of Thrombosis and Haemostasis. 11 (2013) 2 - p. 293-306 , 2013

Link: https://doi.org/10.1111/..

4

Genetics of haemostasis:

GOODEVE, A. C. ; PERRY, D. J. ; CUMMING, T....
Haemophilia. 18 (2012) s4 - p. 73-80 , 2012

Link: https://doi.org/10.1111/..

5

Molecular basis of Bernard-Soulier syndrome in 27 patients ..:

SUMITHA, E. ; JAYANDHARAN, G. R. ; DAVID, S....
Journal of Thrombosis and Haemostasis. 9 (2011) 8 - p. 1590-1598 , 2011

Link: https://doi.org/10.1111/..

6

Quality issues in laboratory haemostasis:

PRESTON, F. E. ; LIPPI, G. ; FAVALORO, E. J....
Haemophilia. 16 (2010) s5 - p. 93-99 , 2010

Link: https://doi.org/10.1111/..

7

Polymorphism in factor VII gene modifies phenotype of sever..:

JAYANDHARAN, G. R. ; NAIR, S. C. ; POONNOOSE, P. M....
Haemophilia. 15 (2009) 6 - p. 1228-1236 , 2009

Link: https://doi.org/10.1111/..

8

A new multiplex PCR and conformation-sensitive gel electrop..:

JAYANDHARAN, G. ; NELSON, E. J. R. ; BAIDYA, S...
Journal of Thrombosis and Haemostasis. 5 (2006) 1 - p. 206-209 , 2006

Link: https://doi.org/10.1111/..

9

Genetic diagnosis of haemophilia and other inherited bleedi..:

PEYVANDI, F. ; JAYANDHARAN, G. ; CHANDY, M....
Haemophilia. 12 (2006) s3 - p. 82-89 , 2006

Link: https://doi.org/10.1111/..

10

Six novel mutations including triple heterozygosity for Phe..:

JAYANDHARAN, G. ; VISWABANDYA, A. ; BAIDYA, S....
Journal of Thrombosis and Haemostasis. 3 (2005) 7 - p. 1482-1487 , 2005

Link: https://doi.org/10.1111/..

11

Molecular genetics of hereditary prothrombin deficiency in ..:

JAYANDHARAN, G. ; VISWABANDYA, A. ; BAIDYA, S....
Journal of Thrombosis and Haemostasis. 3 (2005) 7 - p. 1446-1453 , 2005

Link: https://doi.org/10.1111/..

12

Novel missense mutations in two patients with factor XI def..:

JAYANDHARAN, G. ; SHAJI, R. V. ; NAIR, S. C...
Journal of Thrombosis and Haemostasis. 3 (2005) 4 - p. 808-811 , 2005

Link: https://doi.org/10.1111/..

13

Identification of factor VIII gene mutations in 101 patient..:

Jayandharan, G. ; Shaji, R. V. ; Baidya, S....
Haemophilia. 11 (2005) 5 - p. 481-491 , 2005

Link: https://doi.org/10.1111/..

14

Informativeness of linkage analysis for genetic diagnosis o..:

Jayandharan, G. ; Shaji, R. V. ; George, B...
Haemophilia. 10 (2004) 5 - p. 553-559 , 2004

Link: https://doi.org/10.1111/..

15

Identification of factor IX gene defects using a multiplex ..:

Jayandharan, G. ; Shaji, R. V. ; Chandy, M..
Journal of Thrombosis and Haemostasis. 1 (2003) 9 - p. 2051-2054 , 2003

Link: https://doi.org/10.1046/..