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Results of search for 'au:"Paschali, Ekaterine"'
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Authors
Csoma, Zsanett
Farkas, Katalin
Fábos, Beáta
Kemény, Lajos
Nagy, Katalin
Nagy, Nikoletta
Papp, Ferenc
Paschali, Ekaterine
Sulák, Adrienn
Széll, Márta
Tripolszki, Kornélia
Tóth, Lola
Vályi, Péter
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Topics
Adolescent
Cathepsin C
Child
Child, Preschool
DNA Mutational Analysis
Female
Genetic Predisposition to Disease
Heredity
Heterozygote
Homozygote
Humans
Hungary
Male
Papillon-Lefevre Disease
Pedigree
Phenotype
Sequence Deletion
Skin
Tooth Loss
enzymology
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English
Your search returned 2 results.
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1.
A novel seven-base deletion of the CTSC gene identified in a Hungarian family with Papillon-Lefèvre syndrome.
[electronic resource]
by
Farkas, Katalin
Paschali, Ekaterine
Papp, Ferenc
Vályi, Péter
Széll, Márta
Kemény, Lajos
Nagy, Nikoletta
Csoma, Zsanett
Producer:
20131021
In:
Archives of dermatological research
vol. 305
Online resources:
Available from publisher's website
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2.
CTSC and Papillon-Lefèvre syndrome: detection of recurrent mutations in Hungarian patients, a review of published variants and database update.
[electronic resource]
by
Nagy, Nikoletta
Vályi, Péter
Csoma, Zsanett
Sulák, Adrienn
Tripolszki, Kornélia
Farkas, Katalin
Paschali, Ekaterine
Papp, Ferenc
Tóth, Lola
Fábos, Beáta
Kemény, Lajos
Nagy, Katalin
Széll, Márta
Producer:
20140624
In:
Molecular genetics & genomic medicine
vol. 2
Online resources:
Available from publisher's website
Availability:
No items available.
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