A. Mayerová

发表

Dopamine D3 receptor gene: organization, transcript variants, and polymorphism associated with schizophrenia.

J. Macher, M. Martres, P. Sokoloff, 1996, American journal of medical genetics.

BalI and MspI polymorphisms of the dopamine D3 receptor gene in African Blacks and Caucasians.

J. Macher, A. Buguet, M. Dumas, 1996, Human heredity.

Serological H-Y antigen in the female chicken occurs during gonadal differentiation.

U. Wolf, U. Drews, A. Mayerová, 1988, Differentiation; research in biological diversity.

Phenotypic conversion of human erythrocytes by H-Y antigen

U. Wolf, J. Siebers, U. Müller, 2004, Human Genetics.

Aldosterone deficiency II (CMO II deficiency) is not the result of a mutation of an MspI restriction site within the CYP11B gene

B. Zieger, G. Wolff, M. Brandis, 2005, Human Genetics.

No indication of postnatal selection at the HL-A loci.

K. Bender, A. Mayerová, C. Hiller, 2008, Tissue antigens.

Inverted and satellited Y chromosome in the orangutan (Pongo pygmaeus)

W. Schempp, F. Grützner, W. Rietschel, 1993, Chromosome Research.

Genetic linkage relations of the human plasminogen gene

T. Wienker, S. Bissbort, K. Bender, 2004, Human Genetics.

Sex-reversed XY females with campomelic dysplasia are H-Y negative

J. Lindsten, M. Fraccaro, F. Bricarelli, 2004, Human Genetics.

Association between schizophrenia and homozygosity at the dopamine D3 receptor gene.

D. Collier, P. Sokoloff, J. Schwartz, 1992, Journal of medical genetics.

The occurrence of serological H-Y antigen (Sxs antigen) in the diandric protogynous wrasse, Coris julis (L.) (Labridae, Teleostei).

U. Wolf, A. Mayerová, C. Ebensperger, 1987, Differentiation; research in biological diversity.

Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens

T. Dörk, D. Wieczorek, B. Dworniczak, 1997, Human Genetics.

The X linked recessive form of XY gonadal dysgenesis with a high incidence of gonadal germ cell tumours: clinical and genetic studies.

A. Cameron, J. Mann, V. Woolley, 1983, Journal of medical genetics.

A gene controlling H-Y antigen on the X chromosome

H. Hameister, M. Fraccaro, U. Wolf, 1980, Human Genetics.

Virilization without adrenal hyperplasia in 21-hydroxylase deficiency during fetal life.

H. Dörr, F. Bidlingmaier, G. Wolff, 1984, The Journal of clinical endocrinology and metabolism.

Analysis of the CAG repeats in the SCA1 and B37 genes in schizophrenic and bipolar I disorder patients: tentative association between B37 and schizophrenia.

J. Macher, F. Duval, D. Morris-Rosendahl, 1997, American journal of medical genetics.

Linkage studies in a pedigree with Van der Woude syndrome.

T. Wienker, S. Bissbort, K. Bender, 1987, Journal of medical genetics.

Regional submapping of human chromosome 6 by the use of human-mouse somatic cell hybrids.

K. Grzeschik, K. Bender, A. Mayerová, 1978, Cytogenetics and cell genetics.

Comments on the paper by M. T. Zenzes and T. E. Reed hum genet 66:103–109 (1984)

M. Fraccaro, U. Wolf, U. Müller, 1984, Human Genetics.

Comments on the paper by M.T.Zenzes and T.E.Reed: variability in the amount of serologically detectable H-Y antigen.

M. Fraccaro, U. Wolf, U. Müller, 1984, Human genetics.

Effect of pH, bivalent cations Mg++ and Ca++, trypsin and papain on Tahyna virus.

A. Mayerová, 1966, Acta virologica.

[A significant increase of Tahyña virus neutralizing antibodies in patients with the clinical diagnosis of "acute febrile disease"].

A. Mayerová, V. Mayer, J. Hrúzík, 1966, Ceskoslovenska epidemiologie, mikrobiologie, imunologie.

The Effect of Agar Polyanions and Heparin on the Cytopathic Manifestations of some Arboviruses.

A. Mayerová, 1965 .

IMPROVED PLAQUE ASSAY OF TAHY NA VIRUS (COMPLEX OF CALIFORNIA ENCEPHALITIS).

A. Mayerová, V. Mayer, 1964, Acta virologica.

[A new variant of hemoglobin M].

A. Mayerová, V. Halamová, G. Gvozdjáková, 1970, Ceskoslovenska pediatrie.

C6 LINKAGE STUDIES

T. Wienker, S. Bissbort, K. Bender, 1983, Journal of immunogenetics.

New mutation versus exclusion at the alpha-1-antitrypsin locus: a multifaceted approach in a problematical paternity case.

T. Wienker, J. Epplen, S. Weidinger, 1991, Human heredity.

X-linked genes of the H-Y antigen system in the wood lemming (Myopus schisticolor)

U. Wolf, K. Fredga, U. Müller, 2004, Human Genetics.

Haplotype analysis of the linkage group HLA-A:HLA-B:Bf and its bearing on the interpretation of the linkage disequilibrium

T. Wienker, K. Bender, A. Mayerová, 1977, Human Genetics.

Down's syndrome in twins with discordant HL-A phenotypes

H. Riehm, H. Ritter, K. Bender, 2004, Humangenetik.

Correlation between testicular tissue and H‐Y phenotype in intersex patients

A. Prader, O. Zuffardi, M. Fraccaro, 1983, Clinical genetics.

Absence of Y-specific DNA sequences in human 46,XX true hermaphrodites and in 45,X mixed gonadal dysgenesis

J. Weissenbach, M. Fraccaro, U. Wolf, 1987, Human Genetics.

Presence of H-Y antigen in female patients with sex-chromosome mosaics and absence of testicular tissue.

A. Prader, O. Zuffardi, M. Fraccaro, 1983, American journal of medical genetics.

Clinical reinvestigation and linkage analysis in the family with Episkopi blindness (Norrie disease).

T. Wienker, M. Warburg, P. Ioannou, 1992, Journal of medical genetics.

Haptoglobin types in gypsies from Slovakia (Czechoslovakia).

V. Ferák, M. Vilimova, A. Mayerová, 1969, Human heredity.

SEROLOGICALLY H‐Y ANTIGEN‐NEGATIVE XO MICE

A. Mayerová, U. Wiberg, 1985, Journal of immunogenetics.

Turner syndrome patients are H-Y positive

H. Hameister, O. Zuffardi, M. Fraccaro, 2004, Human Genetics.

Coagulation factor XIII: Genetic linkage studies with F13B

T. Wienker, S. Bissbort, K. Bender, 1987, Genetic epidemiology.

Clinical and functional correlates of a dopamine D3 receptor polymorphism

J. Macher, P. Sokoloff, F. Duval, 1995 .

Correlation between the number of sex chromosomes and the H-Y antigen titer

J. Lindsten, M. Fraccaro, U. Wolf, 2004, Human Genetics.

A male with a monocentric Yq isochromosome and presence of a Yp-specific DNA sequence

M. Schmid, J. Schmidtke, I. Hansmann, 2004, Human Genetics.