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Author
11
Petersen, M. B.
6
Kitsos, G.
4
Iliades, T.
4
Pampanos, A.
4
Psilas, K.
4
Skevas, A.
4
Voyiatzis, N.
3
Aperis, G.
3
Economou-Petersen, E.
3
Eleftheriades, N.
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Female
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Humans
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Pedigree
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*Mutation
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Child, Preschool
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Connexins/*genetics
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DNA Mutational Analysis
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11
journalArticle
Date
8
2000 - 2010
3
1996 - 1999
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ΑΠΟΘΕΤΗΡΙΟ "ΟΛΥΜΠΙΑΣ"
Σχολή Επιστημών Υγείας
Τμήμα Ιατρικής
Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ
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Results 1-10 of 11 (Search time: 0.004 seconds).
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Refining the primary open-angle glaucoma GLC1C region on chromosome 3 by haplotype analysis (Journal article)
Pseudodominant inheritance of DFNB1 deafness due to the common 35delG mutation (Journal article)
Prevalence of GJB2 mutations in prelingual deafness in the Greek population (Journal article)
Prelingual nonsyndromic hearing loss in Greece. Molecular and clinical findings (Journal article)
Primary open angle glaucoma due to T377M MYOC: Population mapping of a Greek founder mutation in Northwestern Greece (Journal article)
Partial trisomy 17q22-qter and partial monosomy Xq27-qter in a girl with a de novo unbalanced translocation due to a postzygotic error: case report and review of the literature on partial trisomy 17qter (Journal article)
FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population (Journal article)
Exclusion of one pedigree affected by adult onset primary open angle glaucoma from linkage to the juvenile glaucoma locus on chromosome 1q21-q31 (Journal article)
Audiological profile of the prevalent genetic form of childhood sensorineural hearing loss due to GJB2 mutations in northern Greece (Journal article)
A novel locus on 19q13 associated with autosomal-dominant macular dystrophy in a large Greek family (Journal article)