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Results of search for 'au:"Klabochová, J"'
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Authors
Al, Taji E
Banghová, K
Cáp, J
Fabianová, J
Goetz, P
Hníková, O
Hurtová, M
Klabochová, J
Kúseková, M
Lebl, J
Losan, F
Novotná, D
Zapletalová, J
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Topics
Adolescent
Adult
Age Factors
Child
Child Development
Child, Preschool
Congenital Hypothyroidism
Female
Goiter
Hearing Loss, Sensorineural
Humans
Hypothyroidism
Infant
Infant, Newborn
Karyotyping
Longitudinal Studies
Male
Membrane Transport Proteins
Mutation
diagnosis
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Czech
Slovak
Your search returned 3 results.
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1.
[Long-term study of children with congenital hypothyroidism].
[electronic resource]
by
Fabianová, J
Klabochová, J
Producer:
19860728
In:
Ceskoslovenska pediatrie
vol. 41
Availability:
No items available.
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2.
[Diagnosis of Turner's syndrome 1965-1989: karyotype, age at diagnosis and determining signs].
[electronic resource]
by
Lebl, J
Goetz, P
Hurtová, M
Klabochová, J
Losan, F
Producer:
19911021
In:
Ceskoslovenska pediatrie
vol. 46
Availability:
No items available.
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3.
[Pendred syndrome among patients with hypothyroidism: genetic diagnosis, phenotypic variability and occurrence of phenocopies].
[electronic resource]
by
Banghová, K
Al, Taji E
Novotná, D
Zapletalová, J
Hníková, O
Cáp, J
Klabochová, J
Kúseková, M
Lebl, J
Producer:
20090319
In:
Casopis lekaru ceskych
vol. 147
Availability:
No items available.
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