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Abnormality of the face
Known as:
Abnormal face
, Abnormality of the physiognomy
, Facial anomaly
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An abnormality of the face. [HPO:probinson]
National Institutes of Health
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Related topics
Related topics
2 relations
Narrower (2)
Congenital anomaly of face
Disorder of face
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2010
Review
2010
The protean visage of systemic autoinflammatory syndromes: a challenge for inter-professional collaboration.
Donato Rigante
European Review for Medical and Pharmacological…
2010
Corpus ID: 46359406
Systemic autoinflammatory syndromes are a group of inherited and acquired disorders of the innate immunity characterized by…
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Review
2009
Review
2009
Tampering with History: Adapting Primary Sources for Struggling Readers.
S. Wineburg
,
Daisy H. Martin
2009
Corpus ID: 59916571
using sources to make history come alive is great in principle, but complicated in practice. consider an example: a teacher wants…
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Review
2002
Review
2002
Objective Facial Motion Analysis in Patients With Facial Nerve Dysfunction
C. Linstrom
The Laryngoscope
2002
Corpus ID: 24030870
Objectives/Hypothesis To objectively measure facial motion at various facial landmarks using a video‐computer interactive system.
Highly Cited
2002
Highly Cited
2002
Clinical Presentation of Allergic Fungal Sinusitis in Children
J. McClay
,
B. Marple
,
+6 authors
N. Schwade
The Laryngoscope
2002
Corpus ID: 39682642
Objective To compare the differences in the clinical and radiographic presentation of allergic fungal sinusitis in children and…
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Highly Cited
2001
Highly Cited
2001
Hemifacial microsomia: Etiology, diagnosis and treatment
R. Monahan
,
Karen Seder
,
P. Patel
,
M. Alder
,
Stephen Grud
,
M. O'gara
2001
Corpus ID: 38996781
ABSTRACT Background Three percent of all newborns have significant structural anomalies. Hemifacial microsomia, or HFM, is the…
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Highly Cited
1997
Highly Cited
1997
Epidemiology of permanent childhood hearing impairment in Trent Region, 1985-1993.
H. Fortnum
,
A. Davis
British Journal of Audiology
1997
Corpus ID: 46499213
This retrospective study of permanent childhood hearing impairment (PCHI) > or = 40 dB HL in children born between 1985 and 1993…
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Highly Cited
1991
Highly Cited
1991
An infant with deletion of the distal long arm of chromosome 15 (q26.1----qter) and loss of insulin-like growth factor 1 receptor gene.
Ellen W. Roback
,
A. Barakat
,
V. Dev
,
M. Mbikay
,
M. Chrétien
,
M. Butler
American journal of medical genetics
1991
Corpus ID: 21875459
We report on an infant with a previously undescribed chromosome 15 deletion (q26.1----qter) and compare the clinical findings…
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Highly Cited
1970
Highly Cited
1970
Hereditary ulnar and fibular dimelia with peculiar facies. A case report.
Richard E. Sandrow
,
Patrick D. Sullivan
,
Howard H. Steel
Journal of Bone and Joint Surgery. American…
1970
Corpus ID: 33641767
A case report of a man with a characteristic facial abnormality, polydactylism of all four extremities, duplication of tarsal and…
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Highly Cited
1950
Highly Cited
1950
Multiple congenital dislocations associated with characteristic facial abnormality.
L. J. Larsen
,
L. J. Larsen
,
+6 authors
F. C. Bost
Jornal de Pediatria
1950
Corpus ID: 39563295
Highly Cited
1939
Highly Cited
1939
Some facial features and their orthodontic implication
M. Hellman
1939
Corpus ID: 73214502
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