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Clinical Genetics|August 1, 1987
Chromosome studies in IgA-deficient patientsR D Taalman, C M Weemaes, T W Hustinx, et al.American Journal of Medical Genetics|March 1, 1989
Further delineation of the Nijmegen breakage syndromeR D Taalman, T W Hustinx, C M Weemaes, et al.American Journal of Medical Genetics|July 1, 1991
Chromosome instability and X-ray hypersensitivity in a microcephalic and growth-retarded childG Barbi, J M Scheres, D Schindler, et al.Cytogenetics and Cell Genetics|May 27, 1999
Sperm analysis in a subfertile male with a Y;16 translocation, using four-color FISHJ C Giltay, P M Kastrop, C H Tiemessen, et al.Cytogenetics and Cell Genetics|January 1, 1997
Assignment of the canalicular multispecific organic anion transporter gene (CMOAT) to human chromosome 10q24 and mouse chromosome 19D2 by fluorescent in situ hybridizationM A van Kuijck, M Kool, G F Merkx, et al.Archives of Dermatological Research|January 1, 1987
Epidermodysplasia verruciformis: Langerhans cells, immunologic effect of retinoid treatment and cytogeneticsP C van Voorst Vader, M C de Jong, R Blanken, et al.Tijdschrift Voor Kindergeneeskunde|August 1, 1984
[Immunologic and cytogenetic aspects of ataxia telangiectasia]C M Weemaes, R D Taalman, P J Van Munster, et al.Cancer Genetics and Cytogenetics|August 1, 1984
Translocation 1;7 in dyshematopoiesis: possibly induced with a nonrandom geographic distributionJ M Scheres, T W Hustinx, R S Holdrinet, et al.Acta Paediatrica Scandinavica|July 1, 1981
A new chromosomal instability disorder: the Nijmegen breakage syndromeC M Weemaes, T W Hustinx, J M Scheres, et al.Annales De Genetique|March 1, 1975
Trisomy 4p in a family with A t(4;15)W J Hustinx, J M Gabreëls, V G Kirkels, et al.Pageof 6