Juho Kärkinen

2PUBLICATIONS
0CO-AUTHORS
Developmental genetics (incl. sex determination)Infant and child health
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Publications (2)

|Apr 28, 2021
Kallmann syndrome in a patient with Weiss-Kruszka syndrome and a de novo deletion in 9q31.2.

Anna-Pauliina Iivonen, Juho Kärkinen, Venkatram Yellapragada

|Oct 27, 2020
Etiology of severe short stature below -3 SDS in a screened Finnish population.

Juho Kärkinen, Päivi J Miettinen, Taneli Raivio

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