Complex morphological and molecular genetic examination of amelogenesis imperfecta: a case presentation of two Czech siblings with a non-syndrome form of the disease.
Neuro Endocrinol Lett
; 35(5): 347-51, 2014.
Article
in En
| MEDLINE
| ID: mdl-25275257
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Dental Enamel
/
Amelogenesis Imperfecta
Type of study:
Diagnostic_studies
/
Screening_studies
Limits:
Child
/
Female
/
Humans
/
Male
Country/Region as subject:
Europa
Language:
En
Journal:
Neuro Endocrinol Lett
Year:
2014
Document type:
Article
Affiliation country:
República Checa
Country of publication:
Suecia