Benign familial hematuria due to mutation of the type IV collagen alpha4 gene.

Por Lemmink, H H, Nillesen, W N, Mochizuki, T, Schröder, C H, Brunner, H G, van Oost, B A, Monnens, L A, Smeets, H J
Publicado em 1996

A novel 3-bp deletion in the PANK2 gene of Dutch patients with pantothenate kinase-associated neurodegeneration: evidence for a founder effect

Por Rump, P., Lemmink, H. H., Verschuuren-Bemelmans, C. C., Grootscholten, P. M., Vos, Y. J., van Essen, A. J., Fock, J. M., Hayflick, S. J., Westaway, S. K.
Publicado em 2005

Novel molecular variants of the Na-K-2Cl cotransporter gene are responsible for antenatal Bartter syndrome.

Por Vargas-Poussou, R, Feldmann, D, Vollmer, M, Konrad, M, Kelly, L, van den Heuvel, L P, Tebourbi, L, Brandis, M, Karolyi, L, Hebert, S C, Lemmink, H H, Deschênes, G, Hildebrandt, F, Seyberth, H W, Guay-Woodford, L M, Knoers, N V, Antignac, C
Publicado em 1998