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Keymolen, K
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1

P-766 A systematic review and standardized clinical validat..:

Petrone, P ; Li Piani, L ; Brutto, M...
Human Reproduction.  39 (2024)  Supplement_1 - p. , 2024
Link: https://doi.org/10.1093/..
 
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2

P-709 Predictive heatmap in Preimplantation Genetic Testing..:

Van Der Kelen, A ; Berckmoes, V ; Keymolen, K...
Human Reproduction.  38 (2023)  Supplement_1 - p. , 2023
Link: https://doi.org/10.1093/..
 
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3

P-773 No impact of cleavage-stage or blastocyst-stage embry..:

Belva, F ; Kondowe, F ; De Vos, A...
Human Reproduction.  38 (2023)  Supplement_1 - p. , 2023
Link: https://doi.org/10.1093/..
 
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4

P-764 Is children's health up to two years of age affected ..:

Belva, F ; Blockeel, C ; Roelants, M...
Human Reproduction.  37 (2022)  Supplement_1 - p. , 2022
Link: https://doi.org/10.1093/..
 
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5

P-552 Analysis of the genomewide BAF profiles of selected S..:

Verdyck, P ; Berckmoes, V ; Keymolen, K..
Human Reproduction.  37 (2022)  Supplement_1 - p. , 2022
Link: https://doi.org/10.1093/..
 
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6

Parameters of poor prognosis in preimplantation genetic tes..:

Van Der Kelen, A ; Santos-Ribeiro, S ; De Vos, A...
Human Reproduction.  36 (2021)  9 - p. 2558-2566 , 2021
Link: https://doi.org/10.1093/..
 
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7

Chromosomal abnormalities after ICSI in relation to semen p..:

Belva, F ; Bonduelle, M ; Buysse, A...
Human Reproduction.  35 (2020)  9 - p. 2149-2162 , 2020
Link: https://doi.org/10.1093/..
 
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8

Preimplantation genetic testing with HLA matching: from cou..:

De Rycke, M. ; De Vos, A. ; Belva, F....
Journal of Human Genetics.  65 (2020)  5 - p. 445-454 , 2020
Link: https://doi.org/10.1038/..
 
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9

ERCC2 mutations in two siblings with a severe trichothiodys..:

Leemans, G. ; De Raeve, L. ; Keymolen, K.
Journal of the European Academy of Dermatology and Venereology.  34 (2020)  4 - p. 876-879 , 2020
Link: https://doi.org/10.1111/..
 
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10

Factors influencing the clinical outcome of preimplantation..:

Berckmoes, V ; Verdyck, P ; De Becker, P...
Human Reproduction.  34 (2019)  5 - p. 949-958 , 2019
Link: https://doi.org/10.1093/..
 
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11

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/..
 
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12

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/..
 
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13

Xeroderma pigmentosum and leukaemia in two sisters:

Pintens, S. ; Pierret, L. ; Keymolen, K...
Journal of the European Academy of Dermatology and Venereology.  30 (2015)  10 - p. , 2015
Link: https://doi.org/10.1111/..
 
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14

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/..
 
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15

PP6.5 – 1922 Incidental findings in array CGH:

Keymolen, K ; De Rademaeker, M ; Van Den Bogaert, A
European Journal of Paediatric Neurology.  17 (2013)  - p. S46 , 2013
Link: https://doi.org/10.1016/..
 
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