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

по Maiburg, M., Alizadeh, B., Kastrop, P., Lock, M., Lans, S., Giltay, J.
Опубликовано 2009

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

по Giltay, J. C., Van Golde, R. J. T., Kastrop, P. M. M.
Опубликовано 2000

Large inv dup(15) chromosome in two generations.

по Van Der Smagt, J J, Giltay, J C, De Ne, J J, Slabbers, G H
Опубликовано 1996

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

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

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

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

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

по 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
Опубликовано в: Pediatr Rheumatol Online J (2015)

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

по 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
Опубликовано в: Pediatr Rheumatol Online J (2015)

De novo variants in CNOT3 cause a variable neurodevelopmental disorder

по 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.
Опубликовано в: Eur J Hum Genet (2019)