E-LIB Suche - Ergebnisse für: Tesi, Bianca

1

Register-based and genetic studies of Prader-Willi syndrome..:

Maya-Gonzalez, Carolina ; Wessman, Sandra ; Lagerstedt-Robinson, Kristina...
Frontiers in Medicine, 2023, 10,. , 2023

2

Cancer risks by sex and variant type in PTEN hamartoma tumo..:

Hendricks, Linda A.J ; Hoogerbrugge, Nicoline ; Mensenkamp, Arjen R...
https://research.rug.nl/en/publications/1cd09805-1429-451f-bbde-05dd7b72e687. , 2023

Link: https://hdl.handle.net/1..

3

P506: CLINICAL VALIDATION OF THE NORDIC GUIDELINES FOR GERM..:

Tesi, Bianca ; Eriksson, Anna ; Baskin, Berivan...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10429588/. , 2023

Link: http://www.ncbi.nlm.nih...

4

Register-based and genetic studies of Prader-Willi syndrome..:

Maya-Gonzalez, Carolina ; Wessman, Sandra ; Lagerstedt-Robinson, Kristina...
Frontiers in Medicine, 2023, 10,. , 2023

Link: http://urn.kb.se/resolve..

5

Cancer risks by sex and variant type in PTEN Hamartoma Tumo..:

Hendricks, Linda A J ; Hoogerbrugge, Nicoline ; Mensenkamp, Arjen R...
info:eu-repo/semantics/altIdentifier/pmid/36171661. , 2023

Link: https://hdl.handle.net/1..

6

Diagnostic Yield From a Nationwide Implementation of Precis..:

Wadensten, Elisabeth ; Wessman, Sandra ; Abel, Frida...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581599/. , 2023

Link: http://www.ncbi.nlm.nih...

7

Genotype-phenotype associations in a large PTEN Hamartoma T..:

Hendricks, Linda A.J ; Hoogerbrugge, Nicoline ; Venselaar, Hanka...
https://research.rug.nl/en/publications/38c4ebc7-996f-4cc5-ab08-34427db3c7c7. , 2022

Link: https://hdl.handle.net/1..

8

Genotype-phenotype associations in a large PTEN Hamartoma T..:

Hendricks, Linda A.J ; Hoogerbrugge, Nicoline ; Venselaar, Hanka...
Reproducció del document publicat a: https://doi.org/10.1016/j.ejmg.2022.104632. , 2022

Link: http://hdl.handle.net/24..

9

Cancer risks by sex and variant type in PTEN hamartoma tumo..:

Hendricks, Linda A. J ; Hoogerbrugge, Nicoline ; Mensenkamp, Arjen R...
Reproducció del document publicat a: https://doi.org/10.1093/jnci/djac188. , 2022

Link: http://hdl.handle.net/24..

10

Genome sequencing is a sensitive first-line test to diagnos..:

Lindstrand, Anna ; Ek, Marlene ; Kvarnung, Malin...
Genetics in Medicine, 1098-3600, 2022, 24:11, s. 2296-2307. , 2022

Link: http://urn.kb.se/resolve..

11

Rubella vaccine–induced granulomas are a novel phenotype wi..:

Gross, Miriam ; Speckmann, Carsten ; May, Annette...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jaci.2021.05.007. , 2021

Link: https://hal.science/hal-..

12

Rubella vaccine–induced granulomas are a novel phenotype wi..:

Gross, Miriam ; Speckmann, Carsten ; May, Annette...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jaci.2021.05.007. , 2021

Link: https://hal.science/hal-..

13

Nordic Guidelines for Germline Predisposition to Myeloid Ne..:

Baliakas, Panagiotis ; Tesi, Bianca ; Wartiovaara-Kautto, Ulla...
10.1097/HS9.0000000000000321. , 2021

Link: http://hdl.handle.net/10..

14

Rubella vaccine–induced granulomas are a novel phenotype wi..:

Gross, Miriam ; Speckmann, Carsten ; May, Annette...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jaci.2021.05.007. , 2021

Link: https://hal.science/hal-..

15

Rubella vaccine–induced granulomas are a novel phenotype wi..:

Groß, Miriam ; Speckmann, Carsten ; May, Annette...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.jaci.2021.05.007. , 2021

Link: https://hal.archives-ouv..