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Journal of Medical Genetics|April 1, 1993
An improved, non-isotopic method of screening cells from patients with abnormalities of sexual differentiation for Y chromosomal DNA contentM Witt, K Michalczak, A Latos-Bielenska, et al.Human Molecular Genetics|January 1, 1993
Illegitimate transcription of the phenylalanine hydroxylase gene in lymphocytes for identification of mutations in phenylketonuriaV Abadie, J Jaruzelska, S Lyonnet, et al.Human Genetics|January 1, 1991
The codon 408 mutation associated with haplotype 2 is predominant in Polish families with phenylketonuriaJ Jaruzelska, K F Henriksen, F Güttler, et al.Journal of Medical Genetics|March 1, 1993
Genetic background of clinical homogeneity of phenylketonuria in PolandJ Jaruzelska, R Matuszak, S Lyonnet, et al.Experimental and Clinical Immunogenetics|January 1, 1993
In situ localization of HLA class I mRNA in human testisM Janitz, D Fiszer, J Jaruzelska, et al.Ginekologia Polska|February 19, 2002
[Importance of cytogenetic analysis in patients with azoospermia or severe oligozoospermia undergoing in vitro fertilization]A Wojda, A Korcz, P Jedrzejczak, et al.Genetics|July 2, 1999
Spatial and temporal distribution of the neutral polymorphisms in the last ZFX intron: analysis of the haplotype structure and genealogyJ Jaruzelska, E Zietkiewicz, M Batzer, et al.Molecular Human Reproduction|January 27, 2009
The highly conserved NANOS2 protein: testis-specific expression and significance for the human male reproductionK M Kusz, L Tomczyk, M Sajek, et al.Molecular Reproduction and Development|December 13, 2006
Polymorphisms of the human PUMILIO2 gene and male sterilityK Kusz, B Ginter-Matuszewska, K Ziolkowska, et al.Journal of Medical Genetics|June 30, 2000
Incomplete masculinisation of XX subjects carrying the SRY gene on an inactive X chromosomeK Kusz, M Kotecki, A Wojda, et al.Pageof 3