E-LIB Suche - Ergebnisse für: Dheedene, Annelies

1

Biallelic RXFP2 variants lead to congenital bilateral crypt..:

Syryn, Hannes ; Van de Velde, Julie ; De Clercq, Griet...
Human Reproduction. , 2024

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

2

Aligning genotyping and copy number data in single trophect..:

De Witte, Lisa ; Baetens, Machteld ; Tilleman, Kelly...
Human Reproduction Open. , 2024

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

3

Haploinsufficiency of ZFHX3, encoding a key player in neuro..:

Pérez Baca, María del Rocío ; Jacobs, Eva Z. ; Vantomme, Lies...
The American Journal of Human Genetics. 111 (2024) 3 - p. 509-528 , 2024

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

4

De novo variants in SP9 cause a novel form of interneuronop..:

Tessarech, Marine ; Friocourt, Gaëlle ; Marguet, Florent...
Genetics in Medicine. 26 (2024) 5 - p. 101087 , 2024

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

5

Expanding the Phenotype of B3GALNT2-Related Disorders:

D'haenens, Erika ; Vergult, Sarah ; Menten, Björn...
Genes. 13 (2022) 4 - p. 694 , 2022

Link: https://doi.org/10.3390/..

6

Performance and Diagnostic Value of Genome-Wide Noninvasive..:

van Riel, Margot ; Brison, Nathalie ; Baetens, Machteld...
Obstetrics & Gynecology. 137 (2021) 6 - p. 1102-1108 , 2021

Link: https://doi.org/10.1097/..

7

Pathogenic variants in CDH11 impair cell adhesion and cause..:

Li, Dong ; March, Michael E. ; Fortugno, Paola...
Human Genetics. 140 (2021) 7 - p. 1061-1076 , 2021

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

8

Outcome of publicly funded nationwide first-tier noninvasiv..:

Van Den Bogaert, Kris ; Lannoo, Lore ; Brison, Nathalie...
Genetics in Medicine. 23 (2021) 6 - p. 1137-1142 , 2021

Link: https://doi.org/10.1038/..

9

Low feasibility of in vitro matured oocytes originating fro..:

Lierman, Sylvie ; Tolpe, Annelies ; De Croo, Ilse...
Fertility and Sterility. 116 (2021) 4 - p. 1068-1076 , 2021

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

10

Phenotypic and Molecular Heterogeneity in Mandibulofacial D..:

Shenoy, Rathika D. ; Shetty, Vikram ; Dheedene, Annelies...
The Cleft Palate-Craniofacial Journal. 59 (2021) 11 - p. 1346-1351 , 2021

Link: https://doi.org/10.1177/..

11

A Reassessment of Copy Number Variations in Congenital Hear..:

Meerschaut, Ilse ; Vergult, Sarah ; Dheedene, Annelies...
Genes. 12 (2021) 7 - p. 1048 , 2021

Link: https://doi.org/10.3390/..

12

Prenatally detected copy number variants in a national coho..:

Muys, Joke ; Jacquemyn, Yves ; Blaumeiser, Bettina...
Prenatal Diagnosis. 40 (2020) 10 - p. 1272-1283 , 2020

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

13

Microcoria due to first duplication of 13q32.1 including th..:

Pozza, Elise ; Verdin, Hannah ; Deconinck, Hilde...
European Journal of Medical Genetics. 63 (2020) 5 - p. 103918 , 2020

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

14

Expanding the molecular spectrum and the neurological pheno..:

Jacobs, Eva Z. ; Brown, Kathleen ; Byler, Melissa C....
Clinical Genetics. 99 (2020) 2 - p. 259-268 , 2020

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

15

PREFACE: In silico pipeline for accurate cell‐free fetal DN..:

Raman, Lennart ; Baetens, Machteld ; De Smet, Matthias...
Prenatal Diagnosis. 39 (2019) 10 - p. 925-933 , 2019

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