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Currarino triad: concurrent US and MRI diagnosis in the fetus and the mother

Prenatal diagnosis, 2002-11, Vol.22 (11), p.1005-1010

2002

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Paracentric inversions of human chromosomes and their risks

Časopis lékařů českých, 2004, Vol.143 (1), p.35

Balícek, P

2004

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Pericentric inversion of human chromosomes and its risks

Časopis lékařů českých, 2001-02, Vol.140 (2), p.38

Balícek, P

2001

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Effect of BrdU on the number of nucleoli and the frequency of satellite associations in PHA-stimulated lymphocytes

Sbornik vedeckych praci Lekarske fakulty Karlovy university v Hradci Kralove, 1988, Vol.31 (5), p.473

Balícek, P

1988

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A somatic origin of homologous Robertsonian translocations and isochromosomes

American journal of human genetics, 1994-02, Vol.54 (2), p.290-302

1994

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Intercalar satellites of human acrocentric chromosomes as a cytological manifestation of polymorphism in GC-rich material?

Human genetics, 1980-01, Vol.54 (3), p.343-347

1980

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RHG-band polymorphism of the short arms of human acrocentric chromosomes and relationship of variants to satellite associations

Human genetics, 1982-01, Vol.62 (3), p.237-239

1982

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INTESTINAL AGANGLIONOSIS IN THE SMITH‐LEMLI‐OPITZ SYNDROME

Acta Paediatrica, 1983-01, Vol.72 (1), p.141-143

1983

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Variability and familial transmission of constitutive heterochromatin of human chromosomes evaluated by the method of linear measurement

Human genetics, 1978-01, Vol.42 (3), p.257-265

1978

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Case reports of patients with a marker chromosome

Časopis lékařů českých, 2004, Vol.143 (10), p.708

2004

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Length of human constitutive heterochromatin in relation to chromosomal contraction

Human genetics, 1977-01, Vol.38 (2), p.189-193

1977

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A case of trisomy 9p in a family with translocation 9/15

Humangenetik, 1975-01, Vol.27 (4), p.353-358

1975

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Cytogenetic analysis of double satellites on marker chromosome No. 14

Sbornik vedeckych praci Lekarske fakulty Karlovy university v Hradci Kralove, 1979, Vol.22 (4), p.331

1979

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Prenatal diagnosis of de novo complex balanced rearrangements in chromosomes 3,4, and 13

Časopis lékařů českých, 2001-03, Vol.140 (4), p.122

2001

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Report on four cases of trisomy 18 syndrome

Sbornik vedeckych praci Lekarske fakulty Karlovy univerzity v Hradci Kralove. Supplementum, 1972, Vol.15 (5), p.521

1972

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Dermatoglyphics of hands in D-G translocation carriers

Sbornik vedeckych praci Lekarske fakulty Karlovy university v Hradci Kralove, 1970, Vol.13 (1), p.41

1970

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The contribution of dermatoglyphic investigation to the diagnosis of the Down syndrome

Sbornik vedeckych praci Lekarske fakulty Karlovy university v Hradci Kralove, 1968, Vol.11 (5), p.769

1968

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Variability of constitutive heterochromatin of human chromosomes in the population. Analysis of sex differences and coincidence of variants

Sbornik vedeckych praci Lekarske fakulty Karlovy university v Hradci Kralove, 1981, Vol.24 (5), p.555

1981

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Chromosomal patterns in patients treated in chronic intermittent haemodialysis programme

Sbornik vedeckych praci Lekarske fakulty Karlovy univerzity v Hradci Kralove. Supplementum, 1979, Vol.22 (1), p.9

1979

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Proceedings: EEG findings in children with Klinefelter's syndrome

Electroencephalography and clinical neurophysiology, 1975-10, Vol.39 (4), p.439-439

1975

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The clinical and cytogenetic manifestations of four cases with partial deletion of the short arm of one of the chromosomes of group B

Sbornik vedeckych praci Lekarske fakulty Karlovy univerzity v Hradci Kralove. Supplementum, 1975, Vol.19 (1), p.167

1975

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Klinefelter's syndrome among offspring of women with triple-X anomaly

Sbornik vedeckych praci Lekarske fakulty Karlovy univerzity v Hradci Kralove. Supplementum, 1975, Vol.19 (1), p.177

1975

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An autoradiographic study of the chromosomes in the cri du chat syndrome

Sbornik vedeckych praci Lekarske fakulty Karlovy university v Hradci Kralove, 1971, Vol.14 (4), p.405

1971

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Trisomy 18 syndrome: analysis of 15 cases

Sbornik vedeckych praci Lekarske fakulty Karlovy university v Hradci Kralove, 1981, Vol.24 (3), p.385

1981

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A boy with 48, XXYY karyotype

Sbornik vedeckych praci Lekarske fakulty Karlovy univerzity v Hradci Kralove. Supplementum, 1975, Vol.19 (1), p.161

1975

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Currarino triad: concurrent US and MRI diagnosis in the fetus and the mother

Paracentric inversions of human chromosomes and their risks

Pericentric inversion of human chromosomes and its risks

Effect of BrdU on the number of nucleoli and the frequency of satellite associations in PHA-stimulated lymphocytes

A somatic origin of homologous Robertsonian translocations and isochromosomes

Intercalar satellites of human acrocentric chromosomes as a cytological manifestation of polymorphism in GC-rich material?

RHG-band polymorphism of the short arms of human acrocentric chromosomes and relationship of variants to satellite associations

INTESTINAL AGANGLIONOSIS IN THE SMITH‐LEMLI‐OPITZ SYNDROME

Variability and familial transmission of constitutive heterochromatin of human chromosomes evaluated by the method of linear measurement

Case reports of patients with a marker chromosome

Length of human constitutive heterochromatin in relation to chromosomal contraction

A case of trisomy 9p in a family with translocation 9/15

Cytogenetic analysis of double satellites on marker chromosome No. 14

Prenatal diagnosis of de novo complex balanced rearrangements in chromosomes 3,4, and 13

Report on four cases of trisomy 18 syndrome

Dermatoglyphics of hands in D-G translocation carriers

The contribution of dermatoglyphic investigation to the diagnosis of the Down syndrome

Variability of constitutive heterochromatin of human chromosomes in the population. Analysis of sex differences and coincidence of variants

Chromosomal patterns in patients treated in chronic intermittent haemodialysis programme

Proceedings: EEG findings in children with Klinefelter's syndrome

The clinical and cytogenetic manifestations of four cases with partial deletion of the short arm of one of the chromosomes of group B

Klinefelter's syndrome among offspring of women with triple-X anomaly

An autoradiographic study of the chromosomes in the cri du chat syndrome

Trisomy 18 syndrome: analysis of 15 cases

A boy with 48, XXYY karyotype

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