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Carolina Maya-González
659
results:
Search for persons
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Format
Online (659)
Mediatypes
E-Books (4)
Articles (Online) (576)
Bookchapter (Online) (30)
OpenAccess-fulltext (49)
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english (475)
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spanish (16)
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1
Diagnostic yield and clinical impact of germline sequencing..:
Tesi, Bianca
;
Robinson, Kristina Lagerstedt
;
Abel, Frida
...
The Lancet Regional Health - Europe. 39 (2024) - p. 100881 , 2024
Link:
https://doi.org/10.1016/..
?
2
Register-based and genetic studies of Prader-Willi syndrome..:
Maya-González, Carolina
;
Wessman, Sandra
;
Lagerstedt-Robinson, Kristina
...
Frontiers in Medicine. 10 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
3
Register-based and genetic studies of Prader-Willi syndrome..:
Carolina Maya-González
;
Sandra Wessman
;
Kristina Lagerstedt-Robinson
...
https://www.frontiersin.org/articles/10.3389/fmed.2023.1172565/full. , 2023
Link:
https://doi.org/10.3389/..
?
4
Data_Sheet_1_Register-based and genetic studies of Prader-W..:
Carolina Maya-González
;
Sandra Wessman
;
Kristina Lagerstedt-Robinson
...
doi:10.3389/fmed.2023.1172565.s001. , 2023
Link:
https://doi.org/10.3389/..
?
5
Table_1_Register-based and genetic studies of Prader-Willi ..:
Carolina Maya-González
;
Sandra Wessman
;
Kristina Lagerstedt-Robinson
...
doi:10.3389/fmed.2023.1172565.s002. , 2023
Link:
https://doi.org/10.3389/..
?
6
Monoallelic and bi-allelic variants in NCDN cause neurodeve..:
Fatima, Ambrin
;
Hoeber, Jan
;
Schuster, Jens
...
The American Journal of Human Genetics. 109 (2022) 3 - p. 542-546 , 2022
Link:
https://doi.org/10.1016/..
?
7
Monoallelic and bi-allelic variants in NCDN cause neurodeve..:
Fatima, Ambrin
;
Hoeber, Jan
;
Schuster, Jens
...
The American Journal of Human Genetics. 108 (2021) 4 - p. 739-748 , 2021
Link:
https://doi.org/10.1016/..
?
8
Incontinentia pigmenti: Generation of an IKBKG deficient hu..:
Fatima, Ambrin
;
Schuster, Jens
;
Akram, Talia
...
Stem Cell Research. 44 (2020) - p. 101739 , 2020
Link:
https://doi.org/10.1016/..
?
9
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..
?
10
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..
?
11
Contributors:
, In:
Factors Affecting Neurodevelopment
,
Albert, Mareike
;
Álvarez-Zaragoza, C.
;
Angulo, Brenda
... - p. xxi-xxv , 2021
Link:
https://doi.org/10.1016/..
?
12
Mono-allelic and bi-allelic variants in NCDN cause neurodev..:
Fatima, Ambrin
;
Hoeber, Jan
;
Schuster, Jens
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2021.02.015. , 2021
Link:
https://hal.sorbonne-uni..
?
13
Mono-allelic and bi-allelic variants in NCDN cause neurodev..:
Fatima, Ambrin
;
Hoeber, Jan
;
Schuster, Jens
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ajhg.2021.02.015. , 2021
Link:
https://hal.sorbonne-uni..
?
14
Incontinentia pigmenti: Generation of an IKBKG deficient hu..:
Ambrin Fatima
;
Jens Schuster
;
Talia Akram
...
http://www.sciencedirect.com/science/article/pii/S187350612030043X. , 2020
Link:
https://doi.org/10.1016/..
?
15
Understanding the conservation-genetics gap in Latin Americ..:
Napolitano, Constanza
;
Clavijo, Cristhian
;
Rojas-Bonzi, Viviana
...
Frontiers in Genetics. 15 (2024) - p. , 2024
Link:
https://doi.org/10.3389/..
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