Faas BH - Search Results

1

Detection of fetal RHD-specific sequences in maternal plasma.

Faas BH, Beuling EA, Christiaens GC, von dem Borne AE, van der Schoot CE. Faas BH, et al. Lancet. 1998 Oct 10;352(9135):1196. doi: 10.1016/s0140-6736(05)60534-x. Lancet. 1998. PMID: 9777844 No abstract available.

2

Genotyping of RHD by multiplex polymerase chain reaction analysis of six RHD-specific exons.

Maaskant-van Wijk PA, Faas BH, de Ruijter JA, Overbeeke MA, von dem Borne AE, van Rhenen DJ, van der Schoot CE. Maaskant-van Wijk PA, et al. Among authors: faas bh. Transfusion. 1998 Nov-Dec;38(11-12):1015-21. doi: 10.1046/j.1537-2995.1998.38111299056309.x. Transfusion. 1998. PMID: 9838930

3

The applicability of different PCR-based methods for fetal RHD and K1 genotyping: a prospective study.

Faas BH, Maaskant-Van Wijk PA, von dem Borne AE, van der Schoot CE, Christiaens GC. Faas BH, et al. Prenat Diagn. 2000 Jun;20(6):453-8. Prenat Diagn. 2000. PMID: 10861708

4

Rapid Rh D genotyping by polymerase chain reaction-based amplification of DNA.

Simsek S, Faas BH, Bleeker PM, Overbeeke MA, Cuijpers HT, van der Schoot CE, von dem Borne AE. Simsek S, et al. Among authors: faas bh. Blood. 1995 May 15;85(10):2975-80. Blood. 1995. PMID: 7742557 Free article.

5

Rh E/e genotyping by allele-specific primer amplification.

Faas BH, Simsek S, Bleeker PM, Overbeeke MA, Cuijpers HT, von dem Borne AE, van der Schoot CE. Faas BH, et al. Blood. 1995 Feb 1;85(3):829-32. Blood. 1995. PMID: 7833484 Free article.

6

The R0Har RH:33 phenotype results from substitution of exon 5 of the RHCE gene by the corresponding exon of the RHD gene.

Beckers EA, Faas BH, von dem Borne AE, Overbeeke MA, van Rhenen DJ, van der Schoot CE. Beckers EA, et al. Among authors: faas bh. Br J Haematol. 1996 Mar;92(3):751-7. doi: 10.1046/j.1365-2141.1996.382918.x. Br J Haematol. 1996. PMID: 8616049

7

Characterization of the hybrid RHD gene leading to the partial D category IIIc phenotype.

Beckers EA, Faas BH, Ligthart P, Simsek S, Overbeeke MA, von dem Borne AE, van Rhenen DJ, van der Schoot CE. Beckers EA, et al. Among authors: faas bh. Transfusion. 1996 Jun;36(6):567-74. doi: 10.1046/j.1537-2995.1996.36696269518.x. Transfusion. 1996. PMID: 8669091

8

Lower antigen site density and weak D immunogenicity cannot be explained by structural genomic abnormalities or regulatory defects of the RHD gene.

Beckers EA, Faas BH, Ligthart P, Overbeeke MA, von dem Borne AE, van der Schoot CE, van Rhenen DJ. Beckers EA, et al. Among authors: faas bh. Transfusion. 1997 Jun;37(6):616-23. doi: 10.1046/j.1537-2995.1997.37697335156.x. Transfusion. 1997. PMID: 9191822

9

Evidence that the RHD(VI) deletion genotype does not exist.

Maaskant-van Wijk PA, Beckers EA, van Rhenen DJ, Mouro I, Colin Y, Cartron JP, Faas BH, van der Schoot CE, Apoil PA, Blancher A, von dem Borne AE. Maaskant-van Wijk PA, et al. Among authors: faas bh. Blood. 1997 Aug 15;90(4):1709-11. Blood. 1997. PMID: 9269793 Free article. No abstract available.

10

Partial expression of RHc on the RHD polypeptide.

Faas BH, Beuling EA, Ligthart PC, van Rhenen DJ, van der Schoot CE. Faas BH, et al. Transfusion. 2001 Sep;41(9):1136-42. doi: 10.1046/j.1537-2995.2001.41091136.x. Transfusion. 2001. PMID: 11552071

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