Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 205,705,626 papers from all fields of science
Search
Sign In
Create Free Account
Otodental Dysplasia
Known as:
Chromosome 11q13 Deletion Syndrome
, Otodental Syndrome
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
9 relations
Autosomal dominant inheritance
Dental Pulp Stone
Taurodontism
Broader (6)
Chromosome Deletion
Chromosomes, Human, Pair 11
Congenital chromosomal disease
Congenital ocular coloboma (disorder)
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2015
Highly Cited
2015
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement
M. Prasad
,
Véronique Geoffroy
,
+52 authors
A. Bloch-Zupan
Journal of Medical Genetics
2015
Corpus ID: 11345945
Background Orodental diseases include several clinically and genetically heterogeneous disorders that can present in isolation or…
Expand
2007
2007
SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma.
C. Gregory‐Evans
,
M. Moosajee
,
+8 authors
K. Gregory-Evans
Human molecular genetics
2007
Corpus ID: 6233985
We ascertained three different families affected with oto-dental syndrome, a rare but severe autosomal-dominant craniofacial…
Expand
Review
2006
Review
2006
Otodental syndrome
A. Bloch-Zupan
,
J. Goodman
Orphanet journal of rare diseases
2006
Corpus ID: 13737001
The otodental syndrome also named otodental dysplasia, is characterised by a striking dental phenotype known as globodontia…
Expand
Review
2001
Review
2001
Otodental syndrome: a case report and genetic considerations.
H. Sedano
,
L. C. Moreira
,
R. A. D. de Souza
,
A. B. Moleri
Oral surgery, oral medicine, oral pathology, oral…
2001
Corpus ID: 40283544
A 5-year-old boy presented with otodental syndrome. His maxillary and mandibular incisors were within normal limits. The premolar…
Expand
1998
1998
Otodental syndrome. A case report.
L. Van Doorne
,
G. Wackens
,
M. De Maeseneer
,
P. Deron
International journal of oral and maxillofacial…
1998
Corpus ID: 7721778
1998
1998
Otodental syndrome: three familial case reports.
L. Santos-Pinto
,
M. Oviedo
,
A. Santos-Pinto
,
H. I. Iost
,
N. Seale
,
A. K. Reddy
Pediatric dentistry
1998
Corpus ID: 28556895
todental syndrome, also named oto-dentodysplasia, ~ otodental 2-4 dysplasia,and globodontia,5’ 6 has been reported as atype of…
Expand
Highly Cited
1987
Highly Cited
1987
Double primary teeth and their relationship with the permanent successors: a radiographic study of 376 cases.
S. Yuen
,
J. Chan
,
S. Wei
Pediatric dentistry
1987
Corpus ID: 27224007
Double primary teeth were observed in 367 children and their relationship with the permanent successors was studied with the aid…
Expand
1983
1983
The association of ocular defects with the otodental syndrome.
Winter Gb
1983
Corpus ID: 77108489
1981
1981
Otodental Dysplasia: a Five Year Study
R. Cook
,
J. Cox
,
R. Jorgenson
Ear and hearing
1981
Corpus ID: 2595465
Peripheral auditory sensitivity is documented over a 5-year period on 4 cases with otodental dysplasia. Age of onset is noted for…
Expand
1976
1976
Globodontia in the otodental syndrome.
C. Witkop
,
K. Gundlach
,
W. J. Streed
,
J. Sauk
Oral surgery, oral medicine, and oral pathology
1976
Corpus ID: 11638381
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
,
Terms of Service
, and
Dataset License
ACCEPT & CONTINUE