-
-
저자
손정민
최남기
김선미
양규호
-
제어번호
75056234
-
학술지명
大韓小兒齒科學會誌
-
권호사항
Vol.
34
No.
4
[
2007
]
-
발행처
大韓小兒齒科學會
-
발행처 URL
http://www.kapd.org
-
자료유형
학술저널
-
수록면
658-665
-
언어
Korean
-
출판년도
2007
-
KDC
515
-
등재정보
KCI등재
-
판매처
'
부분 무치증 환아의 증례보고' 의 주제별 논문영향력
논문영향력 요약
주제 |
|
동일주제 총논문수 |
논문피인용 총횟수 |
주제별 논문영향력의 평균 |
906
|
0
|
|
주제별 논문영향력
논문영향력
주제 |
주제별 논문수 |
주제별 피인용횟수 |
주제별 논문영향력 |
주제분류(KDC/DDC) |
치과의학, 이비인후과학, 안과 ...
|
906
|
0
|
|
계 |
|
906
|
0
|
|
* 다른 주제어 보유 논문에서 피인용된 횟수 |
0
|
|
'
부분 무치증 환아의 증례보고' 의 참고문헌
-
-
-
supernumerary teeth and fused teeth in the primary dentition
-
-
The prevalence of malocclusion in Swedish schoolchildren
-
The genetics of human tooth agenesis: new discoveries for understanding dental anomalies 117
650 ~ 656
[2000]
-
The genetics of human tooth agenesis: New discoveries for understanding dental anomalies
-
Studies on Pax9-Msx1 protein interactions
-
Simultaneous occurrence of unusual odontodysplasia and oligodontia in the permanent dentition: report of a case
-
Signs and symptoms from ectodermal organs in young Swedish individuals with oligodontia
-
Reported prevalence of congenitally missing teeth in two Norwegian counties
-
Radiographic manifestations of an unusual combination Types I and Type II dentin dysplasia
-
Radiographic assessment of congenitally missing teeth in orthodontic patients
-
-
Oligodontia in Danish schoolchildren
-
Numerical variations in primary dentition and their correlation with the permanent dentition
-
Mutations in AXIN2 cause familial tooth agenesis and predispose to colorectal cancer
-
Hypodontia in orthodontically treated children
-
Hereditary defects of dentin
-
Exclusion of coding region mutations in MSX1, PAX9 and AXIN2 in eight patients with severe oligodontia phenotype
김재복
Exclusion of coding region mutations in MSX1
[2006]
-
Distribution of missing teeth and tooth morphology in patients with oligodontia
-
Dentinal dysplasia type I: report of a case
-
Congenital dental anormalies occuring in 3
-
Clinician’s view of hypodontia
-
Clinical, radiographic, and genetic evaluation of a novel form of autosomal-dominant oligodontia
-
Absence of mutations in the homeodomain of the MSX1 gene in patients with hypodontia
-
A unique form of hypodontia seen in Vietnamese patients: clinical and molecular analysis
-
A survey of hypodontia in Japanese orthodontic patients
-
A proposed classification for heritable human dentine defects with a description of a new entity
-
A case of dentinal dysplasia
'
부분 무치증 환아의 증례보고'
의 유사주제(
) 논문