Search Results - "Mayerova, A."

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  1. 1

    Association between schizophrenia and homozygosity at the dopamine D3 receptor gene by Crocq, M A, Mant, R, Asherson, P, Williams, J, Hode, Y, Mayerova, A, Collier, D, Lannfelt, L, Sokoloff, P, Schwartz, J C

    Published in Journal of medical genetics (01-12-1992)
    “…Disturbances in dopamine neurotransmission have been postulated to underlie schizophrenia. We report data from two independent studies of a BalI polymorphism…”
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  2. 2

    The occurrence of serological H-Y antigen (Sxs antigen) in the diandric protogynous wrasse, Coris julis (L.) (Labridae, Teleostei) by Reinboth, R, Mayerová, A, Ebensperger, C, Wolf, U

    Published in Differentiation (London) (01-01-1987)
    “…The serological sex-specific (Sxs) antigen (previously called 'H-Y antigen') has been shown, in various vertebrate species ranging from fish to mammals, to be…”
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  3. 3

    Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens by DÖRK, T, DWORNICZAK, B, PANDER, H.-J, SPERLING, H, RATJEN, F, PASSARGE, E, SCHMIDTKE, J, STUHRMANN, M, AULEHLA-SCHOLZ, C, WIECZOREK, D, BÖHM, I, MAYEROVA, A, SEYDEWITZ, H. H, NIESCHLAG, E, MESCHEDE, D, HORST, J

    Published in Human genetics (01-09-1997)
    “…Congenital absence of the vas deferens (CAVD) is a frequent cause for obstructive azoospermia and accounts for 1%-2% of male infertility. A high incidence of…”
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  4. 4

    Dopamine D3 receptor gene: Organization, transcript variants, and polymorphism associated with schizophrenia by Griffon, N., Crocq, M. A., Pilon, C., Martres, M. P., Mayerova, A., Uyanik, G., Burgert, E., Duval, F., Macher, J. P., Javoy-Agid, F., Tamminga, C. A., Schwartz, J. C., Sokoloff, P.

    Published in American journal of medical genetics (16-02-1996)
    “…DNA fragments from a genomic library were used to establish the partial structure of the human dopamine D3 receptor gene (DRD3). Its coding sequence contains 6…”
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    A male with a monocentric Yq isochromosome and presence of a Yp-specific DNA sequence by SCHMIDTKE, J, ARNEMANN, J, SCHMID, M, BAUM, F, MAYEROVA, A, LANGENBECK, U, HANSMANN, I

    Published in Human genetics (01-01-1985)
    “…We describe clinical features and laboratory findings in a physically and mentally retarded male with underdeveloped testes, a seemingly monocentric…”
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    Serologically H-Y antigen-negative XO mice by Wiberg, U H, Mayerová, A

    Published in Journal of immunogenetics (01-02-1985)
    “…In a series of six independent experiments organ homogenates of 35 mice of the XX, XO or XY sex chromosome constitutions were absorbed using three different…”
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  9. 9

    On regional mapping of human chromosome 6. Review and own findings by Bender, K, Bissbort, S, Hiller, C, Mayerova, A, Wienker, T F

    Published in Acta anthropogenetica (1983)
    “…In addition to the committee Reports on the Constitution of Chromosome 6 also the mapping contributions from patients with no. 6 imbalances were added to the…”
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    Epidemic of acute haemorrhagic conjunctivitis in Freetown, Sierra Leone, in 1970 by Bagar, B, Cummings, E C, Mayerová, A

    “…Epidemiological features of the epidemic of acute haemorrhagic conjunctivitis in Freetown, Sierra Leone, in 1970, are described. On the basis of hospital…”
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  12. 12

    H-Y antigen in human X-autosome translocations by Mayerova, A, Zuffardi, O, Maraschio, P, Muller, U, Sperling, K, Ropers, H H, Fraccaro, M, Wolf, U

    Published in Acta anthropogenetica (1983)
    “…The distal segment of the X chromosome short arm (Xp223) escapes X-inactivation in the normal female. This was shown by the activity of three genes assigned to…”
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    Clinical reinvestigation and linkage analysis in the family with Episkopi blindness (Norrie disease) by Wolff, G, Mayerová, A, Wienker, T F, Atalianis, P, Ioannou, P, Warburg, M

    Published in Journal of medical genetics (01-11-1992)
    “…We present the results of a clinical and genetic reinvestigation of the Cypriot family affected by an X chromosomally inherited eye disease originally…”
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  15. 15

    Presence of H-Y antigen in female patients with sex-chromosome mosaics and absence of testicular tissue by Müller, U, Mayerova, A, Fraccaro, M, Zuffardi, O, Mikkelsen, M, Prader, A

    Published in American journal of medical genetics (01-06-1983)
    “…H-Y antigen was tested in five women with sex chromosome mosaicism and gonadal streaks. Three patients had a 45,X/46,XY or 46,X,der(Y) and two a 45,X/46,X,…”
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  16. 16

    Assignment of the gene coding for human catalase to the short arm of chromosome 11 by Wieacker, P, Mueller, C R, Mayerova, A, Grzeschik, K H, Ropers, H H

    Published in Annales de génétique (1980)
    “…Human and murine catalases can be separated electrophoretically as single bands of different mobility. In man-mouse somatic cell hybrids, however, detection of…”
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  17. 17

    New mutation versus exclusion at the alpha-1-antitrypsin locus: a multifaceted approach in a problematical paternity case by Bender, K, Kasulke, D, Mayerovà, A, Hummel, K, Weidinger, S, Epplen, J T, Wienker, T F

    Published in Human heredity (01-01-1991)
    “…In a case of disputed paternity with overwhelming indications of fatherhood for the putative father, as supported by serological tests and biostatistical…”
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    Linkage studies in a pedigree with Van der Woude syndrome by Wienker, T F, Hudek, G, Bissbort, S, Mayerová, A, Mauff, G, Bender, K

    Published in Journal of medical genetics (01-03-1987)
    “…A kindred segregating for Van der Woude syndrome (VWS) through five generations is described. Biochemical and serological phenotypes at 36 polymorphic marker…”
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  20. 20

    Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesis by WAIBEL, F, SCHERER, G, FRACCARO, M, HUSTINX, T. W. J, WEISSENBACH, J, WIELAND, J, MAYEROVA, A, BACK, E, WOLF, U

    Published in Human genetics (01-08-1987)
    “…A search for Y-specific DNA sequences has been performed in a sample of seven 46,XX true hermaphrodites and one 45,X mixed gonadal dysgenesis case and compared…”
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