E-LIB Suche - Ergebnisse für: Aagaard Nolting, Line

1

Novel biallelic PISD missense variants cause spondyloepimet..:

Aagaard Nolting, Line ; Holling, Tess ; Nishimura, Gen...
Clinical Genetics. , 2024

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

2

A new 1p36.13‐1p36.12 microdeletion syndrome characterized ..:

Aagaard Nolting, Line ; Brasch‐Andersen, Charlotte ; Cox, Helen...
Clinical Genetics. 97 (2020) 6 - p. 927-932 , 2020

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

3

A new 1p36.13-1p36.12 microdeletion syndrome characterized ..:

Aagaard Nolting, Line ; Brasch-Andersen, Charlotte ; Cox, Helen...
Aagaard Nolting , L , Brasch-Andersen , C , Cox , H , Kanani , F , Parker , M , Fry , A E , Loddo , S , Novelli , A , Dentici , M L , Joss , S , Jørgensen , J P & Fagerberg , C R 2020 , ' A new 1p36.13-1p36.12 microdeletion syndrome characterized by learning disability, behavioral abnormalities, and ptosis ' , Clinical Genetics , vol. 97 , no. 6 , pp. 927-932 . https://doi.org/10.1111/cge.13739. , 2020

Link: https://portal.findresea..

4

Association of candidate pharmacogenetic markers with plati..:

Langer, Thorsten ; Clemens, Eva ; Broer, Linda...
Data in Brief. 32 (2020) - p. 106227 , 2020

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

5

Usefulness of current candidate genetic markers to identify..:

Langer, Thorsten ; Clemens, Eva ; Broer, Linda...
European Journal of Cancer. 138 (2020) - p. 212-224 , 2020

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