Klapecki, Jakub

Instytut Matki i Dziecka

1 paper on CoChatORCID 0000-0003-2236-6903

Most cited papers

Verified
Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1
Gregor, A., Albrecht, B., Bader, I., Bijlsma, E. K., Ekici, A. B., Engels, H., Hackmann, K., Horn, D., Hoyer, J., Klapecki, J., et al. (2011) · BMC Medical Genetics
Genetics and Neurodevelopmental DisordersGenomic variations and chromosomal abnormalities
Cited by 121

Go further with a free account

Verify every reference, keep papers in a library, and ask questions across them.

Sign up - it is free