Millar DS - Search Results

1

Prenatal exclusion of severe factor VII deficiency.

Ariffin H, Millar DS, Cooper DN, Chow T, Lin HP. Ariffin H, et al. Among authors: millar ds. J Pediatr Hematol Oncol. 2003 May;25(5):418-20. doi: 10.1097/00043426-200305000-00014. J Pediatr Hematol Oncol. 2003. PMID: 12759632

2

Prenatal exclusion of haemophilia A and carrier testing by direct detection of a disease lesion.

Schwartz M, Cooper DN, Millar DS, Kakkar VV, Scheibel E. Schwartz M, et al. Among authors: millar ds. Prenat Diagn. 1992 Nov;12(11):861-6. doi: 10.1002/pd.1970121103. Prenat Diagn. 1992. PMID: 1362983

3

Prenatal exclusion of severe factor VII deficiency by DNA sequencing.

Millar DS, Cooper DN, Kakkar VV, Schwartz M, Scheibel E. Millar DS, et al. Lancet. 1992 May 30;339(8805):1359. doi: 10.1016/0140-6736(92)92005-z. Lancet. 1992. PMID: 1350022 No abstract available.

4

Molecular analysis of the genotype-phenotype relationship in factor VII deficiency.

Millar DS, Kemball-Cook G, McVey JH, Tuddenham EG, Mumford AD, Attock GB, Reverter JC, Lanir N, Parapia LA, Reynaud J, Meili E, von Felton A, Martinowitz U, Prangnell DR, Krawczak M, Cooper DN. Millar DS, et al. Hum Genet. 2000 Oct;107(4):327-42. doi: 10.1007/s004390000373. Hum Genet. 2000. PMID: 11129332

5

A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal Purpura fulminans: prenatal diagnosis in an at-risk pregnancy.

Millar DS, Allgrove J, Rodeck C, Kakkar VV, Cooper DN. Millar DS, et al. Blood Coagul Fibrinolysis. 1994 Aug;5(4):647-9. Blood Coagul Fibrinolysis. 1994. PMID: 7841323

6

Carrier detection in haemophilia A by direct analysis of factor VIII gene lesions.

Millar DS, Green PJ, Zoll B, Kakkar VV, Cooper DN. Millar DS, et al. Hum Genet. 1991 May;87(1):99-100. doi: 10.1007/BF01213104. Hum Genet. 1991. PMID: 1903760

7

Molecular genetic analysis of factor X deficiency: gene deletion and germline mosaicism.

Wieland K, Millar DS, Grundy CB, Mibashan RS, Kakkar VV, Cooper DN. Wieland K, et al. Among authors: millar ds. Hum Genet. 1991 Jan;86(3):273-8. doi: 10.1007/BF00202408. Hum Genet. 1991. PMID: 1997381

8

Inherited factor VII deficiency: molecular genetics and pathophysiology.

Cooper DN, Millar DS, Wacey A, Banner DW, Tuddenham EG. Cooper DN, et al. Among authors: millar ds. Thromb Haemost. 1997 Jul;78(1):151-60. Thromb Haemost. 1997. PMID: 9198146 Review. No abstract available.

9

Molecular genetic analysis of severe protein C deficiency.

Millar DS, Johansen B, Berntorp E, Minford A, Bolton-Maggs P, Wensley R, Kakkar V, Schulman S, Torres A, Bosch N, Cooper DN. Millar DS, et al. Hum Genet. 2000 Jun;106(6):646-53. doi: 10.1007/s004390000315. Hum Genet. 2000. PMID: 10942114

10

The molecular genetics of haemophilia A: screening for point mutations in the factor VIII gene using the restriction enzyme TaqI.

Millar DS, Zoll B, Martinowitz U, Kakkar VV, Cooper DN. Millar DS, et al. Hum Genet. 1991 Sep;87(5):607-12. doi: 10.1007/BF00209022. Hum Genet. 1991. PMID: 1840568

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