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Ret proto-oncogene mutation found in the Czech population and its predictive value for offspring of patients with medullary carcinoma of the thyroid gland

Vnitřní lékar̆stvĭ, 1996-11, Vol.42 (11), p.751

1996

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Chromosome markers and balanced translocation in the etiology of infertility

Ceská gynekologie, 1998-02, Vol.63 (1), p.51

1998

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Chromosome polymorphism

Bratislavské lékarské listy, 1985-06, Vol.83 (6), p.620

1985

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Partial trisomy 1q25-1q32 in a boy with isolated lactase deficiency

Československá pediatrie, 1990-02, Vol.45 (2), p.87

1990

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The fragile X chromosome syndrome

Československá pediatrie, 1987-11, Vol.42 (11), p.650

1987

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Familial occurrence of translocation between chromosomes No. 3 and 4

Časopis lékařů českých, 1979-01, Vol.118 (3), p.73

1979

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Clinical and molecular problems in polycystic kidneys

Časopis lékařů českých, 1990-01, Vol.129 (2), p.36

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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Familial occurence of abnormal karyotype 14p

Sbornik vedeckych praci Lekarske fakulty Karlovy univerzity v Hradci Kralove. Supplementum, 1975, Vol.19 (1), p.155

1975

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Autoradiographic analysis of familial D-D translocation

Československá pediatrie, 1972-11, Vol.27 (11), p.545

1972

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Initial experience with the diagnosis of hemophilia A using molecular genetics

Časopis lékařů českých, 1987-05, Vol.126 (22), p.682

1987

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Family occurrence of translocation DqDqt (13q 14q) (author's transl)

Sbornik lekarsky, 1974-05, Vol.76 (4), p.131

1974

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Familial incidence of pericentric inversion of X chromosome

Československá pediatrie, 1974-05, Vol.29 (5), p.245

1974

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Genetic aspect of the dyslexic child

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

1970

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Peutz-Jeghers syndrome in 6 children

Československá pediatrie, 1970-03, Vol.25 (3), p.132

Sabacký, J

1970

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Translocation forms of Down's disease. (Ethical problems in the search for translocation carriers)

Československá pediatrie, 1970-04, Vol.25 (4), p.181

1970

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Manifestations of genetic burden in prenatal and postnatal periods

Československá pediatrie, 1972-06, Vol.27 (6), p.261

1972

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Recent clinical and genetic aspects ensuing from the study of the heterogenous character of alpha-amylase

Ceskoslovenska gastroenterologie a vyziva, 1972-10, Vol.26 (7), p.324

Kamarýt, J

1972

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Familial incidence of Down's disease

Československá pediatrie, 1973-02, Vol.28 (2), p.81

1973

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Dyschromatopsy in twins

Sbornik lekarsky, 1971-03, Vol.73 (3), p.57

1971

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Prenatal diagnosis of the carrier of the translocation form of Down's disease

Ceskoslovenska gynekologie, 1972-06, Vol.37 (6), p.433

1972

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Ret proto-oncogene mutation found in the Czech population and its predictive value for offspring of patients with medullary carcinoma of the thyroid gland

Chromosome markers and balanced translocation in the etiology of infertility

Chromosome polymorphism

Partial trisomy 1q25-1q32 in a boy with isolated lactase deficiency

The fragile X chromosome syndrome

Familial occurrence of translocation between chromosomes No. 3 and 4

Clinical and molecular problems in polycystic kidneys

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

Familial occurence of abnormal karyotype 14p

Autoradiographic analysis of familial D-D translocation

Initial experience with the diagnosis of hemophilia A using molecular genetics

Family occurrence of translocation DqDqt (13q 14q) (author's transl)

Familial incidence of pericentric inversion of X chromosome

Genetic aspect of the dyslexic child

Peutz-Jeghers syndrome in 6 children

Translocation forms of Down's disease. (Ethical problems in the search for translocation carriers)

Manifestations of genetic burden in prenatal and postnatal periods

Recent clinical and genetic aspects ensuing from the study of the heterogenous character of alpha-amylase

Familial incidence of Down's disease

Dyschromatopsy in twins

Prenatal diagnosis of the carrier of the translocation form of Down's disease

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