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Nayebzadeh, Naemeh
7  Ergebnisse:
Personensuche X
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1

Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and..:

Kaustio, Meri ; Nayebzadeh, Naemeh ; Hinttala, Reetta...
Journal of Allergy and Clinical Immunology.  148 (2021)  2 - p. 599-611 , 2021
Link: https://doi.org/10.1016/..
 
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2

Biallelic loss-of-function P4HTM gene variants cause hypoto..:

Rahikkala, Elisa ; Myllykoski, Matti ; Hinttala, Reetta...
Genetics in Medicine.  21 (2019)  10 - p. 2355-2363 , 2019
Link: https://doi.org/10.1038/..
 
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3

Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and..:

Kaustio, Meri ; Nayebzadeh, Naemeh ; Hinttala, Reetta...
NFR/187615.  , 2022
Link: http://hdl.handle.net/10..
 
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4

Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and..:

Kaustio, Meri ; Nayebzadeh, Naemeh ; Hinttala, Reetta...
10.1016/j.jaci.2020.12.656.  , 2021
Link: http://hdl.handle.net/10..
 
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5

Biallelic loss-of-function P4HTM gene variants cause hypoto..:

Rahikkala, Elisa ; Myllykoski, Matti ; Hinttala, Reetta...
10.1038/s41436-019-0503-4.  , 2019
Link: http://hdl.handle.net/10..
 
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6

Loss of DIAPH1 causes SCBMS, combined immunodeficiency, and..:

Kaustio, M. (Meri) ; Nayebzadeh, N. (Naemeh) ; Hinttala, R. (Reetta)... , 2021
Link: http://urn.fi/urn:nbn:fi..
 
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7

Biallelic loss-of-function P4HTM gene variants cause hypoto..:

Rahikkala, E. (Elisa) ; Myllykoski, M. (Matti) ; Hinttala, R. (Reetta)... , 2019
Link: http://urn.fi/urn:nbn:fi..
 
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