E-LIB Suche - Ergebnisse für: Sandkuyl, L. A.

1

Sharing of a conserved haplotype suggests a susceptibility ..:

Hillert, J. ; He, B. ; Giedraitis, V....
Journal of Neuroimmunology. 90 (1998) 1 - p. 104 , 1998

Link: https://doi.org/10.1016/..

2

The lipoprotein lipase (ASN291→SER) mutation is associated ..:

Hoffer, M.J.V. ; Bredie, S.J.H. ; Boomsma, D.I....
Atherosclerosis. 115 (1995) - p. S21 , 1995

Link: https://doi.org/10.1016/..

3

Association of particular HLA class II alleles, haplotypes ..:

Buyse, I. ; Sandkuyl, L. A. ; Zamani Ghabanbasani, M....
Diabetologia. 37 (1994) 8 - p. 808-817 , 1994

Link: https://doi.org/10.1007/..

4

The mutation ΔF508 on Dutch cystic fibrosis chromosomes: fr..:

Halley, D. J. J. ; Veeze, H. J. ; Sandkuyl, L. A....
Human Genetics. 85 (1990) 4 - p. 407-408 , 1990

Link: https://doi.org/10.1007/..

5

Risk calculation of missed prenatal diagnosis of fragile‐X ..:

Oostra, B. A. ; Sandkuyl, L. A. ; Halley, D. J. J.
Prenatal Diagnosis. 10 (1990) 8 - p. 545-546 , 1990

Link: https://doi.org/10.1002/..

6

Identification of a closely linked DNA marker, DXS178, to f..:

Kwan, Sau-Ping ; Terwilliger, J. ; Parmley, R....
Genomics. 6 (1990) 2 - p. 238-242 , 1990

Link: https://doi.org/10.1016/..

7

Genetic heterogeneity in tuberous sclerosis:

Janssen, L.A.J. ; Sandkuyl, L.A. ; Merkens, E.C....
Genomics. 8 (1990) 2 - p. 237-242 , 1990

Link: https://doi.org/10.1016/..

8

Tissue-Specific Splicing Mutation in Acute Intermittent Por..:

Grandchamp, B. ; Picat, C. ; Mignotte, V....
Proceedings of the National Academy of Sciences of the United States of America. 86 (1989) 2 - p. 661-664 , 1989

Link: https://www.jstor.org/st..

9

Polyclonal hyper-immunoglobulin G1(A1) syndrome: Evidence f..:

Hendriks, R. W. ; Sandkuyl, L. A. ; Kraakman, M. E. M...
Human Genetics. 82 (1989) 2 - p. 194-196 , 1989

Link: https://doi.org/10.1007/..

10

Tissue-specific splicing mutation in acute intermittent por..:

Grandchamp, B ; Picat, C ; Mignotte, V...
Proceedings of the National Academy of Sciences. 86 (1989) 2 - p. 661-664 , 1989

Link: https://doi.org/10.1073/..

11

Assignment of autosomal dominant spinocerebellar ataxia cen..:

Zoghbi, H.Y. ; Sandkuyl, L.A. ; Ott, J....
Human Immunology. 23 (1988) 2 - p. 161 , 1988

Link: https://doi.org/10.1016/..

12

Early diagnosis in X-linked agammaglobulinaemia:

Schuurman, R. K. B. ; Mensink, E. J. B. M. ; Sandkuyl, L. A...
European Journal of Pediatrics. 147 (1988) 1 - p. 93-95 , 1988

Link: https://doi.org/10.1007/..

13

X-linked immunodeficiency with hyperimmunoglobulinemia M ap..:

Mensink, E.J.B.M. ; Thompson, A. ; Sandkuyl, L.A....
Human Genetics. 76 (1987) 1 - p. , 1987

Link: https://doi.org/10.1007/..

14

Mapping of a gene for X-linked agammaglobulinemia and evide..:

Mensink, E. J. B. M. ; Thompson, A. ; Schot, J. D. L....
Human Genetics. 73 (1986) 4 - p. 327-332 , 1986

Link: https://doi.org/10.1007/..

15

The absolute quantification of human IgM and IgG: Standardi..:

De Bruyn, A.M. ; Klein, F. ; Neumann, H....
Journal of Immunological Methods. 48 (1982) 3 - p. 339-348 , 1982

Link: https://doi.org/10.1016/..