Nowaczyk, Stéphanie
17  Ergebnisse:
Personensuche X
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2

Expanded phenotypic spectrum of neurodevelopmental and neur..:

Layo-Carris, Dana E ; Lubin, Emily E ; Sangree, Annabel K...
https://discovery.ucl.ac.uk/id/eprint/10191954/1/s41431-024-01610-1.pdf.  , 2024
 
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3

Evaluation of multiple transcriptomic gene risk signatures ..:

Bayani, Jane ; Poncet, Coralie ; Crozier, Cheryl...
Bayani , J , Poncet , C , Crozier , C , Neven , A , Piper , T , Cunningham , C , Sobol , M , Aebi , S , Benstead , K , Bogler , O , Dal Lago , L , Fraser , J , Hilbers , F , Hedenfalk , I , Korde , L , Linderholm , B , Martens , J , Middleton , L , Murray , M , Kelly , C , Nilsson , C , Nowaczyk , M , Peeters , S , Peric , A , Porter , P , Schröder , C , Rubio , I T , Ruddy , K J , van Asperen , C , Van Den Weyngaert , D , van Deurzen , C , van Leeuwen-Stok , E , Vermeij , J , Winer , E , Giordano , S H , Cardoso , F & Bartlett , J M S 2021 , ' Evaluation of multiple transcriptomic gene risk signatures in male breast cancer ' , npj Breast Cancer , vol. 7 , no. 1 , 98 . https://doi.org/10.1038/s41523-021-00301-0.  , 2021
 
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4

Evaluation of multiple transcriptomic gene risk signatures ..:

Bayani, Jane ; Poncet, Coralie ; Crozier, Cheryl...
https://pure.eur.nl/en/publications/c0108411-8b28-4fe6-a4b2-a9db38e67086.  , 2021
 
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5

Evaluation of multiple transcriptomic gene risk signatures ..:

Bayani, Jane ; Poncet, Coralie ; Crozier, Cheryl...
https://research.rug.nl/en/publications/a5175111-2ac1-4cdf-8fa2-ec2c32ffab41.  , 2021
 
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7

Metadata record for the article: Evaluation of multiple tra..:

Jane Bayani (79733) ; Coralie Poncet (10822351) ; Cheryl Crozier (9338415)...
https://figshare.com/articles/online_resource/Metadata_record_for_the_article_Evaluation_of_multiple_transcriptomic_gene_risk_signatures_in_male_breast_cancer/14616831.  , 2021
 
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14

The phenotype of Floating-Harbor syndrome : clinical charac..:

Nikkel, Sarah M ; Dauber, Andrew ; De Munnik, Sonja...
Nikkel et al.: The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP. Orphanet Journal of Rare Diseases 2013 8:63..  , 2013
 
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