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Results of search for 'au:"Havlovicová, M"'
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Authors
Balícek, P
Baxová, A
Bóday, A
Cernáková, I
Drábová, J
Franková, V
Geryk, J
Goetz, P
Havlovicová, M
Holubová, A
Hrdlicka, M
Kocárek, E
Konrádová, V
Krejcová, S
Krutílková, V
Křepelová, A
Losan, F
Musová, Z
Novotná, D
Sedlácek, Z
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Topics
Abnormalities, Multiple
Adenomatous Polyposis Coli
Adolescent
Adult
Autistic Disorder
Breast Neoplasms
Child
Child, Preschool
Chromosome Aberrations
Chromosome Fragility
Female
Genetic Predisposition to Disease
Humans
Infant
Male
Mutation
Neoplasms
Phenotype
diagnosis
genetics
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Languages
Czech
English
Your search returned 7 results.
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1.
[Genetics of autism].
[electronic resource]
by
Sedlácek, Z
Havlovicová, M
Hrdlicka, M
Producer:
20021001
In:
Casopis lekaru ceskych
vol. 141
Availability:
No items available.
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2.
[Specialized genetic counseling in pediatric and adult oncology patients].
[electronic resource]
by
Krutílková, V
Havlovicová, M
Goetz, P
Producer:
20020404
In:
Casopis lekaru ceskych
vol. 141
Availability:
No items available.
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3.
[Psychosocial factors associated with genetic testing for certain hereditary types of neoplasms].
[electronic resource]
by
Franková, V
Zidovská, J
Krutílková, V
Havlovicová, M
Goetz, P
Producer:
20040108
In:
Casopis lekaru ceskych
vol. 142
Availability:
No items available.
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4.
[Genetic study of 20 patients with autism disorders].
[electronic resource]
by
Havlovicová, M
Propper, L
Novotná, D
Musová, Z
Hrdlicka, M
Sedlácek, Z
Producer:
20021001
In:
Casopis lekaru ceskych
vol. 141
Availability:
No items available.
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5.
[DNA diagnosis of the fragile X chromosome syndrome--FRAXA using PCR].
[electronic resource]
by
Bóday, A
Mat'oska, V
Konrádová, V
Havlovicová, M
Musová, Z
Krejcová, S
Seemanová, E
Producer:
19980409
In:
Casopis lekaru ceskych
vol. 137
Availability:
No items available.
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6.
[Case reports of patients with a marker chromosome].
[electronic resource]
by
Kocárek, E
Novotná, D
Maríková, T
Cernáková, I
Losan, F
Balícek, P
Baxová, A
Havlovicová, M
Goetz, P
Producer:
20050106
In:
Casopis lekaru ceskych
vol. 143
Availability:
No items available.
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7.
Molecular genetic analysis in 14 Czech Kabuki syndrome patients is confirming the utility of phenotypic scoring.
[electronic resource]
by
Paděrová, J
Holubová, A
Simandlová, M
Puchmajerová, A
Vlčková, M
Malíková, M
Pourová, R
Vejvalková, S
Havlovicová, M
Šenkeříková, M
Ptáková, N
Drábová, J
Geryk, J
Maver, A
Křepelová, A
Macek, M
Producer:
20170630
In:
Clinical genetics
vol. 90
Online resources:
Available from publisher's website
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No items available.
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