Mibashan RS - Search Results

1

Prenatal diagnosis of haemoglobinopathies by ion exchange HPLC of haemoglobins.

Rouyer-Fessard P, Plassa F, Blouquit Y, Vidaud M, Varnavides L, Mibashan RS, Bellingham A, Beuzard Y. Rouyer-Fessard P, et al. Among authors: mibashan rs. Prenat Diagn. 1989 Jan;9(1):19-26. doi: 10.1002/pd.1970090104. Prenat Diagn. 1989. PMID: 2473467

2

Prenatal diagnosis of beta thalassaemia by reverse phase HPLC.

Rouyer-Fessard P, Beuzard Y, Vidaud M, John P, Mibashan RS. Rouyer-Fessard P, et al. Among authors: mibashan rs. Prenat Diagn. 1987 Mar;7(3):171-8. doi: 10.1002/pd.1970070304. Prenat Diagn. 1987. PMID: 3588537

3

The molecular genetic analysis of hemophilia A: a directed search strategy for the detection of point mutations in the human factor VIII gene.

Pattinson JK, Millar DS, McVey JH, Grundy CB, Wieland K, Mibashan RS, Martinowitz U, Tan-Un K, Vidaud M, Goossens M, et al. Pattinson JK, et al. Among authors: mibashan rs. Blood. 1990 Dec 1;76(11):2242-8. Blood. 1990. PMID: 1979502 Free article.

4

Normal blood cell values in the early mid-trimester fetus.

Millar DS, Davis LR, Rodeck CH, Nicolaides KH, Mibashan RS. Millar DS, et al. Among authors: mibashan rs. Prenat Diagn. 1985 Nov-Dec;5(6):367-73. doi: 10.1002/pd.1970050602. Prenat Diagn. 1985. PMID: 4088972

5

Prenatal diagnosis of hereditary protein C deficiency.

Mibashan RS, Millar DS, Rodeck CH, Nicolaides KH, Berger A, Seligsohn U. Mibashan RS, et al. N Engl J Med. 1985 Dec 19;313(25):1607. doi: 10.1056/NEJM198512193132513. N Engl J Med. 1985. PMID: 3840865 No abstract available.

6

Selective feticide of the affected twin by fetoscopic air embolism.

Rodeck CH, Mibashan RS, Abramowicz J, Campbell S. Rodeck CH, et al. Among authors: mibashan rs. Prenat Diagn. 1982 Jul;2(3):189-94. doi: 10.1002/pd.1970020308. Prenat Diagn. 1982. PMID: 7145847

7

The molecular genetic analysis of haemophilia A; characterization of six partial deletions in the factor VIII gene.

Millar DS, Steinbrecher RA, Wieland K, Grundy CB, Martinowitz U, Krawczak M, Zoll B, Whitmore D, Stephenson J, Mibashan RS, et al. Millar DS, et al. Among authors: mibashan rs. Hum Genet. 1990 Dec;86(2):219-27. doi: 10.1007/BF00197709. Hum Genet. 1990. PMID: 2125022

8

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: mibashan rs. Hum Genet. 1991 Jan;86(3):273-8. doi: 10.1007/BF00202408. Hum Genet. 1991. PMID: 1997381

9

Improved carrier detection of haemophilia A using novel RFLPs at the DXS115 (767) locus.

Jedlicka P, Greer S, Millar DS, Grundy CB, Jenkins E, Mitchell M, Mibashan RS, Kakkar VV, Cooper DN. Jedlicka P, et al. Among authors: mibashan rs. Hum Genet. 1990 Aug;85(3):315-8. doi: 10.1007/BF00206753. Hum Genet. 1990. PMID: 1697559

10

Fetal haemophilia and allied bleeding disorders.

Mibashan RS, Millar DS. Mibashan RS, et al. Br Med Bull. 1983 Oct;39(4):392-8. doi: 10.1093/oxfordjournals.bmb.a071853. Br Med Bull. 1983. PMID: 6416347 Review. No abstract available.

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