E-LIB Suche - Ergebnisse für: Stouffs, K.

1

PB0986 Genotype-Phenotype Correlation in Belgian Patients w..:

Bouteille, S. ; Stouffs, K. ; Jochmans, K..
Research and Practice in Thrombosis and Haemostasis. 7 (2023) - p. 101804 , 2023

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

2

OC 17.3 Prothrombotic Polymorphisms FV Leiden and Prothromb..:

Bravo Perez, C. ; Orlando, C. ; Gindele, R....
Research and Practice in Thrombosis and Haemostasis. 7 (2023) - p. 100627 , 2023

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

3

O-184 Maternally inherited differences in mitochondrial DNA..:

Mertens, J ; Belva, F ; Van Montfoort, A...
Human Reproduction. 36 (2021) Supplement_1 - p. , 2021

Link: https://doi.org/10.1093/..

4

EP08.24: Malformations of cortical development: from prenat..:

Garofalo, G. ; Marangoni, M. ; Jansen, A....
Ultrasound in Obstetrics & Gynecology. 54 (2019) S1 - p. 284-284 , 2019

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

5

Expanding the clinical spectrum of biallelic ZNF335 variant:

Stouffs, K. ; Stergachis, A.B. ; Vanderhasselt, T....
Clinical Genetics. 94 (2018) 2 - p. 246-251 , 2018

Link: https://doi.org/10.1111/..

6

Are AZFb deletions always incompatible with sperm productio..:

Stouffs, K. ; Vloeberghs, V. ; Gheldof, A...
Andrology. 5 (2017) 4 - p. 691-694 , 2017

Link: https://doi.org/10.1111/..

7

Complex phenotype associated with mutation in the TANGO2 ge..:

De Meirleir, L. ; D'Hooghe, M. ; De Rademaeker, M....
European Journal of Paediatric Neurology. 21 (2017) - p. e60 , 2017

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

8

Detailed molecular characterization of a novel IDS exonic m..:

Grodecká, L. ; Kováčová, T. ; Kramárek, M....
Journal of Molecular Medicine. 95 (2016) 3 - p. 299-309 , 2016

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

9

OP10 – 2707: Childhood-onset ataxic gait solved by muscle b..:

Jansen, A. ; Ceuterick-de Groote, C. ; Vanderhasselt, T....
European Journal of Paediatric Neurology. 19 (2015) - p. S4 , 2015

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

10

PP05.6 – 2896: Genotype-phenotype correlations and counseli..:

Keymolen, K. ; Stouffs, K. ; Gheldof, A....
European Journal of Paediatric Neurology. 19 (2015) - p. S47-S48 , 2015

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

11

P137 – 2976: Two cases of Noonan syndrome: Genotype–phenoty..:

De Rademaeker, M. ; Jansen, A. ; Gies, I....
European Journal of Paediatric Neurology. 19 (2015) - p. S132 , 2015

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

12

Array comparative genomic hybridization in male infertility:

Stouffs, K. ; Vandermaelen, D. ; Massart, A....
Human Reproduction. 27 (2012) 3 - p. 921-929 , 2012

Link: https://doi.org/10.1093/..

13

Mutation analysis of three genes in patients with maturatio..:

Stouffs, K. ; Vandermaelen, D. ; Tournaye, H...
Reproductive BioMedicine Online. 22 (2011) 1 - p. 65-71 , 2011

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

14

Male infertility and the involvement of the X chromosome:

Stouffs, K. ; Tournaye, H. ; Liebaers, I..
Human Reproduction Update. 15 (2009) 6 - p. 623-637 , 2009

Link: https://doi.org/10.1093/..

15

Do we need to search for gr/gr deletions in infertile men i..:

Stouffs, K. ; Tournaye, H. ; Van der Elst, J....
Human Reproduction. 23 (2008) 5 - p. 1193-1199 , 2008

Link: https://doi.org/10.1093/..