Does the genetic and familial background of males undertaking ICSI affect the outcome?

av Maiburg, M., Alizadeh, B., Kastrop, P., Lock, M., Lans, S., Giltay, J.
Publicerad 2009

Analysis of Spermatozoa from Seven ICSI Males with Constitutional Sex Chromosomal Abnormalities by Fluorescent In Situ Hybridization

av Giltay, J. C., Van Golde, R. J. T., Kastrop, P. M. M.
Publicerad 2000

Large inv dup(15) chromosome in two generations.

av Van Der Smagt, J J, Giltay, J C, De Ne, J J, Slabbers, G H
Publicerad 1996

Polymorphic detection of a parthenogenetic maternal and double paternal contribution to a 46,XX/46,XY hermaphrodite.

av Giltay, J C, Brunt, T, Beemer, F A, Wit, J M, van Amstel, H K, Pearson, P L, Wijmenga, C
Publicerad 1998

The parent-of-origin of the extra X chromosome may differentially affect psychopathology in Klinefelter syndrome

av Bruining, H., van Rijn, S, Swaab, H, Giltay, J., Kates, W., Kas, M. J. H., van Engeland, H, de Sonneville, L
Publicerad 2010

A novel mutation in NLRC4 in a large pedigree with an anakinra responsive autoinflammatory disease

av Volker-Touw, N, de Koning, H, van Kempen, T, Oberndorff, K, van Steensel, M, Giltay, J, Boes, M, de Kovel, C, Simon, A, Frenkel, J, van Gijn, M
I publikationen Pediatr Rheumatol Online J (2015)

Phenotypic variability in patients with ADA2 deficiency due to identical homozygous R169Q mutations

av Van Montfrans, J, Hartman, E, Braun, K, Hennekam, F, Hak, A, Nederkoorn, P, Westendorp, W, Bredius, R, Kollen, W, Scholvinck, E, Legger, G, Meyts, I, Liston, A, Lichtenbelt, K, Giltay, J, Van Haaften, G, De Vries Simons, G, Leavis, H, Nierkens, S, Sanders, C, Van Gijn, M
I publikationen Pediatr Rheumatol Online J (2015)

De novo variants in CNOT3 cause a variable neurodevelopmental disorder

av Martin, R., Splitt, M., Genevieve, D., Aten, E., Collins, A., de Bie, C. I., Faivre, L., Foulds, N., Giltay, J., Ibitoye, R., Joss, S., Kennedy, J., Kerr, B., Kivuva, E., Koopmans, M., Newbury-Ecob, R., Jean-Marçais, N., Peeters, E. A. J., Smithson, S., Tomkins, S., Tranmauthem, F., Piton, A., van Haeringen, A.
I publikationen Eur J Hum Genet (2019)