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Mutagenic effect of advanced paternal age in neurocardiofaciocutaneous syndrome

Časopis lékařů českých, 2014, Vol.153 (5), p.242

2014

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Clinical relevance of chromosomal aberrations in bone and soft tissue tumors in children and young adults

Klinická onkologie, 2009, Vol.22 (2), p.58-66

2009

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Molecular genetic study of causes of the Prader-Willi and Angelman syndrome

Časopis lékařů českých, 2005, Vol.144 (2), p.113-118

2005

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Microdeletion syndromes

Časopis lékařů českých, 2002-06, Vol.141 (12), p.363

Seemanová, E

2002

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Analysis of the most frequent mutations in girls with Rett syndrome

Časopis lékařů českých, 2001-08, Vol.140 (15), p.473

2001

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A boy with a 49,XXXXY karyotype, case report

Československá pediatrie, 1990-09, Vol.45 (9), p.562

1990

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What do the chromosome-breakage syndromes teach us about the care of persons at increased risk for malignant diseases?

Časopis lékařů českých, 1986-07, Vol.125 (30), p.921

German, J

1986

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The importance of cytogenetic examination in childhood malignancies

Československá pediatrie, 1990-03, Vol.45 (3), p.146

1990

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X chromosome-linked lymphoproliferative syndrome (Duncan's disease)

Časopis lékařů českých, 1990-02, Vol.129 (8), p.247

1990

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The 47,XXX syndrome in a family with the fragile X chromosome syndrome

Časopis lékařů českých, 1985-08, Vol.124 (31), p.988

1985

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Similarity between the syndrome of partial trisomy of the long arm of chromosome 3 and the Cornelia de Lange syndrome

Československá pediatrie, 1988-12, Vol.43 (12), p.723

1988

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A case of 45,XO/46,X,r(X). A brief clinical communication

Sbornik lekarsky, 1987-02, Vol.89 (2-3), p.73

1987

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Genetic problems in mentally retarded children

Československá pediatrie, 1981-04, Vol.36 (4), p.206

Kucerová, M

1981

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Pericentric inversion of chromosome 9 in 2 families with an additional type of chromosome aberration

Sbornik vedeckych praci Lekarske fakulty Karlovy univerzity v Hradci Kralove. Supplementum, 1976, Vol.19 (5), p.603

1976

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Genetic aspect of the dyslexic child

Československá pediatrie, 1970-03, Vol.25 (3), p.135

1970

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Klinefelter's syndrome--clinical and laboratory findings in 5 boys

Československá pediatrie, 1974-04, Vol.29 (4), p.198

1974

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The fragile chromosome X syndrome

Časopis lékařů českých, 1982-10, Vol.121 (40), p.1238

1982

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Frequency and distribution of satellites in the parents of children with numerical chromosome aberrations in comparison with parents of healthy children

Bratislavské lékarské listy, 1972-11, Vol.58 (5), p.517

1972

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Clinical manifestation of mosaicism XO/XY (author's transl)

Bratislavské lékarské listy, 1976, Vol.66 (3), p.339

1976

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The fluoroangiographic picture of sex-linked hereditary retinoschisis

Ceskoslovenska oftalmologie, 1987-09, Vol.43 (5), p.342

1987

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Changes in lymphocyte tissue cultures in infectious hepatitis

Vnitřní lékar̆stvĭ, 1970-09, Vol.16 (9), p.833

1970

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Differential diagnosis of syndromes with dysgenesis and agenesis of gonads

Ceskoslovenska gynekologie, 1973-04, Vol.38 (3), p.201

Jirásek, J E

1973

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Current problems in the treatment and ambulatory care of genetic diseases in gynecology and obstetrics

Ceskoslovenska gynekologie, 1972-12, Vol.37 (9), p.661

1972

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Genealogic study of discoid lupus erythematosus. Siblings and children of probands

Sbornik lekarsky, 1971-04, Vol.73 (4), p.99

1971

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Mutagenic effect of advanced paternal age in neurocardiofaciocutaneous syndrome

Clinical relevance of chromosomal aberrations in bone and soft tissue tumors in children and young adults

Molecular genetic study of causes of the Prader-Willi and Angelman syndrome

Microdeletion syndromes

Analysis of the most frequent mutations in girls with Rett syndrome

A boy with a 49,XXXXY karyotype, case report

What do the chromosome-breakage syndromes teach us about the care of persons at increased risk for malignant diseases?

The importance of cytogenetic examination in childhood malignancies

X chromosome-linked lymphoproliferative syndrome (Duncan's disease)

The 47,XXX syndrome in a family with the fragile X chromosome syndrome

Similarity between the syndrome of partial trisomy of the long arm of chromosome 3 and the Cornelia de Lange syndrome

A case of 45,XO/46,X,r(X). A brief clinical communication

Genetic problems in mentally retarded children

Pericentric inversion of chromosome 9 in 2 families with an additional type of chromosome aberration

Genetic aspect of the dyslexic child

Klinefelter's syndrome--clinical and laboratory findings in 5 boys

The fragile chromosome X syndrome

Frequency and distribution of satellites in the parents of children with numerical chromosome aberrations in comparison with parents of healthy children

Clinical manifestation of mosaicism XO/XY (author's transl)

The fluoroangiographic picture of sex-linked hereditary retinoschisis

Changes in lymphocyte tissue cultures in infectious hepatitis

Differential diagnosis of syndromes with dysgenesis and agenesis of gonads

Current problems in the treatment and ambulatory care of genetic diseases in gynecology and obstetrics

Genealogic study of discoid lupus erythematosus. Siblings and children of probands

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