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The interaction of the polymorphisms in transporter of antigen peptides (TAP) and lymphotoxin α (LT-α) genes and atopic diseases in the Czech population

Clinical and experimental allergy, 2001-09, Vol.31 (9), p.1418-1423

2001

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Congenital lymphedema and monosomy X (author's transl)

Bratislavské lékarské listy, 1979-11, Vol.72 (5), p.530

Izakovic, V

1979

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The interaction of the polymorphisms in transporter of antigen peptides (TAP) and lymphotoxin a (LT-α) genes and atopic diseases in the Czech population

Clinical and experimental allergy, 2001, Vol.31 (9), p.1418-1423

2001

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Gonadal dysgenesis in two sisters with male nuclear sex pattern and female characteristics in polymorphonuclear leukocytes

The journal of clinical endocrinology and metabolism, 1960-09, Vol.20, p.1301-1303

IZAKOVIC, V

1960

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Mosaicism 45,X/46,XX in two sisters

The journal of clinical endocrinology and metabolism, 1969-06, Vol.29 (6), p.863-863

Izakovic, V

1969

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Clonal evolution of karyotype in blastic phase of CML

Neoplasma, 1982, Vol.29 (5), p.613

1982

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Research on nuclear sex characteristics of mature segmented neutrophil leukocytes in enriched blood smears

Endokrinologie, 1960-10, Vol.39, p.274

1960

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Chronic lymphoproliferative disease of large granular lymphocytes

Neoplasma, 1988, Vol.35 (1), p.81

1988

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Karyotype of peripheral blood and bone marrow cells in Fanconi's anaemia (author's transl)

Bratislavské lékarské listy, 1977-10, Vol.68 (4), p.424

1977

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Monosomy X associate with fra(17p12) and 22p

Clinical genetics, 1984-01, Vol.26 (2), p.165-166

Izakovic, V

1984

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Werner's syndrome in two siblings (author's transl)

Bratislavské lékarské listy, 1981-01, Vol.75 (1), p.75

1981

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Zum Fremdsprachenunterricht in der technischen Fachorientierung (Englisch) (L'enseignement des langues étrangères dans le domaine des techniques (l'anglais))

Zeitschrift für Phonetik, Sprachwissenschaft und Kommunikationsforschung, 1982, Vol.35 (4), p.476-479

IZAKOVIC, V

1982

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Congenital dyserythropoietic anaemia (author's transl)

Bratislavské lékarské listy, 1978-05, Vol.69 (5), p.589

1978

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Spontaneous puberty followed by precocious menopause in two girls with X monosomy (author's transl)

Bratislavské lékarské listy, 1975-05, Vol.63 (5), p.602

1975

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Homozygosity for fragile site at 17p12 in a 28-year-old healthy man

Human genetics, 1984-01, Vol.68 (4), p.340-341

IZAKOVIC, V

1984

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Karyotype 45, XX, --11,2q+ of bone marrow cells in a case of di Guglielmo syndrome

Folia haematologica (Leipzig, Germany : 1928), 1977, Vol.104 (4), p.533

1977

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Short stature and karyotype of mitotic cells in women

Endokrinologie, 1972-02, Vol.59 (2), p.265

1972

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Monosomy X associated with fra(17p12) and 22p

Clinical genetics, 1984-08, Vol.26 (2), p.165-166

Izakovic, V

1984

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Antitumorous therapy and its consequences upon gravidity and foetus (author's transl)

Ceskoslovenska gynekologie, 1979-05, Vol.44 (4), p.272

1979

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Waldenstrom's macroglobulinaemia. II. Some properties of blood serum proteins

Neoplasma, 1960, Vol.7, p.48

1960

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Karyotype of mitotic cells in haematopoietic diseases

Review of Czechoslovak medicine, 1974, Vol.20 (2), p.49

1974

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An unusual form of adrenogenital syndrome

Endokrinologie, 1971-04, Vol.57 (3), p.343

1971

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Females with gonosome complement XY. II. Pure gonadal dysgenesis with karyotype 46, XY

Bratislavské lékarské listy, 1972-03, Vol.57 (3), p.341

Izakovic, V

1972

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Females with gonosomal complement XY. I. Testicular feminization syndrome

Bratislavské lékarské listy, 1971, Vol.56 (2), p.231

Izakovic, V

1971

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Structural anomalies of chromosome X Deletion of chromosome X ("minute chromosome")-Xf, isochromosome X-Xqui,?Xpi and ring chromosome X-Xr

Bratislavské lékarské listy, 1970-03, Vol.53 (3), p.284

Izakovic, V

1970

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The interaction of the polymorphisms in transporter of antigen peptides (TAP) and lymphotoxin α (LT-α) genes and atopic diseases in the Czech population

Congenital lymphedema and monosomy X (author's transl)

The interaction of the polymorphisms in transporter of antigen peptides (TAP) and lymphotoxin a (LT-α) genes and atopic diseases in the Czech population

Gonadal dysgenesis in two sisters with male nuclear sex pattern and female characteristics in polymorphonuclear leukocytes

Mosaicism 45,X/46,XX in two sisters

Clonal evolution of karyotype in blastic phase of CML

Research on nuclear sex characteristics of mature segmented neutrophil leukocytes in enriched blood smears

Chronic lymphoproliferative disease of large granular lymphocytes

Karyotype of peripheral blood and bone marrow cells in Fanconi's anaemia (author's transl)

Monosomy X associate with fra(17p12) and 22p

Werner's syndrome in two siblings (author's transl)

Zum Fremdsprachenunterricht in der technischen Fachorientierung (Englisch) (L'enseignement des langues étrangères dans le domaine des techniques (l'anglais))

Congenital dyserythropoietic anaemia (author's transl)

Spontaneous puberty followed by precocious menopause in two girls with X monosomy (author's transl)

Homozygosity for fragile site at 17p12 in a 28-year-old healthy man

Karyotype 45, XX, --11,2q+ of bone marrow cells in a case of di Guglielmo syndrome

Short stature and karyotype of mitotic cells in women

Monosomy X associated with fra(17p12) and 22p

Antitumorous therapy and its consequences upon gravidity and foetus (author's transl)

Waldenstrom's macroglobulinaemia. II. Some properties of blood serum proteins

Karyotype of mitotic cells in haematopoietic diseases

An unusual form of adrenogenital syndrome

Females with gonosome complement XY. II. Pure gonadal dysgenesis with karyotype 46, XY

Females with gonosomal complement XY. I. Testicular feminization syndrome

Structural anomalies of chromosome X Deletion of chromosome X ("minute chromosome")-Xf, isochromosome X-Xqui,?Xpi and ring chromosome X-Xr

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