Männik, K
130  Ergebnisse:
Personensuche X
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3

A novel de novo 1.8 Mb microdeletion of 17q21.33 associated..:

Preiksaitiene, E. ; Männik, K. ; Dirse, V....
European Journal of Medical Genetics.  55 (2012)  11 - p. 656-659 , 2012
 
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4

Maternally and paternally inherited deletion of 7q31 involv..:

Žilina, O. ; Reimand, T. ; Zjablovskaja, P....
American Journal of Medical Genetics Part A.  158A (2011)  1 - p. 254-256 , 2011
 
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5

Possible association of 16p11.2 copy number variation with ..:

Giannuzzi, G ; Chatron, N ; Mannik, K...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41525-022-00308-x.  , 2022
 
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9

Rare variants in the genetic background modulate cognitive ..:

Pizzo, L ; Jensen, M ; Polyak, A...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41436-018-0266-3.  , 2019
 
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10

Rare variants in the genetic background modulate cognitive ..:

Pizzo L ; Jensen M ; Polyak A...
info:eu-repo/semantics/altIdentifier/pmid/30190612.  , 2019
 
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11

The Human-Specific BOLA2 Duplication Modifies Iron Homeosta..:

Giannuzzi G ; Schmidt P. J ; Porcu E...
info:eu-repo/semantics/altIdentifier/pmid/31668704.  , 2019
 
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14

CNV-association meta-analysis in 191,161 European adults re..:

Mace, A ; Tuke, MA ; Deelen, P...
https://discovery.ucl.ac.uk/id/eprint/10098119/1/s41467-017-00556-x.pdf.  , 2017
 
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15

CNV-association meta-analysis in 191,161 European adults re..:

Macé, A ; Tuke, MA ; Deelen, P...
https://openaccess.sgul.ac.uk/id/eprint/109020/40/s41467-017-00556-x.pdf.  , 2017
 
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