Tamminga S., Stalman S.E., Kamp G.A., Hendriks Y.M., Knegt A.C., Elting M.W.,

Maternal uniparental disomy 14 – Differential diagnosis with Prader Willi syndrome

Ned. Tijdschrift Geneeskd. 2015;159:A8240.


Tamminga S, van Schendel RV, Rommers W, Bilardo C.M, Pajkrt E, Dondorp WJ, van

Maarle M, Cornel MC, Henneman L. Changing to NIPT as a first-tier screening test and

future perspectives: Opinions of health professionals. Prenat. Diagn. 2015 Dec;35(13):1316-23


Tamminga S., van Maarle M, Henneman L, Oudejans CBM, Cornel MC, Sistermans

EA. Maternal plasma DNA and RNA sequencing. Adv. Clin. Chem. 2016;74:63-102