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

1

Transinguinal preperitoneal (TIPP) vs endoscopic total extr..:

Posthuma, J. J. ; Sandkuyl, R. ; Sloothaak, D.A....
Hernia. 27 (2022) 1 - p. 119-125 , 2022

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

2

Transinguinal preperitoneal (TIPP) vs endoscopic total extr..:

Posthuma, J. J ; Sandkuyl, R ; Sloothaak, D.A...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9931826/. , 2022

Link: http://www.ncbi.nlm.nih...

3

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/..

4

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/..

5

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/..

6

Mapping of facioscapulohumeral muscular dystrophy gene to c..:

Wijmenga, Cisca ; Padberg, George W. ; Moerer, Petra...
Genomics. 9 (1991) 4 - p. 570-575 , 1991

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

7

Progress in the search for genetic linkage with Tourette sy..:

Pakstis, Andrew J ; Heutink, Peter ; Pauls, David L...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1683024. , 1991

Link: http://www.ncbi.nlm.nih...

8

Diagnosis of Wiskott-Aldrich syndrome by analysis of the X ..:

Hendriks, R W ; De Weers, M ; Mensink, R G...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1535400. , 1991

Link: http://www.ncbi.nlm.nih...

9

An Attempt to Map Two Genes for Tuberous Sclerosis Using No..:

POVEY, S ; ATTWOOD, J ; JANSSEN, LAJ...
qt9t86d8c2. , 1991

Link: https://escholarship.org..

10

A Comparative Study on Genetic Heterogeneity in Tuberous Sc..:

JANSSEN, LAJ ; POVEY, S ; ATTWOOD, J...
qt6r63j272. , 1991

Link: https://escholarship.org..

11

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/..

12

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/..

13

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/..

14

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/..

15

Genetic mapping of X-linked albinism-deafness syndrome (ADF..:

Shiloh, Yosef ; Litvak, Gilad ; Ziv, Yael...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1683749. , 1990

Link: http://www.ncbi.nlm.nih...