Skip to search formSkip to main contentSkip to account menu

Eyebrow structure

Known as: Eyebrows, Set of eyebrows, Eyebrow 
Curved rows of HAIR located on the upper edges of the eye sockets.
National Institutes of Health

Related topics

Related topics

11 relations
Atrophoderma vermiculatumHeadMicrobiologicalSet of accessory visual structures

Narrower (3)

Burnett Schwartz Berberian syndromeEyebrows duplication of, with stretchable skin and syndactylyICHTHYOSIS--CHEEK--EYEBROW SYNDROME

Broader (1)

Hair

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
1997
1997
A Fully Automatic Approach to Facial Feature Detection and Tracking
The detection of facial features is a necessary step for a wide range of applications e.g. person verification, lipreading and… 
1991
1991
A malformed child with a recombinant chromosome 7, rec(7) dup p, derived from a maternal pericentric inversion inv(7)(p15q36).
We report a child with facial dysmorphic features, hypoplasia of the external genitalia, intestinal malrotation, congenital… 
1986
1986
Deletion 14q(q24.3 to q32.1) syndrome: significance of peculiar facial appearance in its diagnosis, and deletion mapping of (α1-antitrypsin)
SummaryA 10-month-old Japanese boy who had interstitial deletion of the long arm of chromosome No. 14; 46,XY, del(14)(pter»q24.3… 
Review
1982
Review
1982
The Forehead-Brow Lift
The forehead-brow lift, though generally thought to achieve very little and for only a brief time, corrects ptosis of the… 
Review
1976
Review
1976
RECONSTRUCTION OF EYELIDS AND EYEBROWS IN BURNED PATIENTS
The records of 283 consecutive patients treated for facial burns were reviewed. Eighteen percent of these patients had… 
Highly Cited
1975
Highly Cited
1975
Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).
Close phenotypic similarity between two cases carrying a rec(3) dup q,inv(3) (p25q21), 12 additional infants from the same inv (3… 
1975
1975
Familial partial trisomy of the long arm of chromosome 10 (q24-26).
Two fourth cousins with a strikingly similar pattern of malformation and who have an unbalanced translocation (46, XY, -17, +t… 
1973
1973
Segregating Reciprocal (4;21) (q21;q21) Translocation with Proposita Trisomic for Parts of 4q and 21
The segregation of a balanced reciprocal (4;21)(q21;q21) translocation is described. The family was ascertained through a… 
Highly Cited
1964
Highly Cited
1964
WAARDENBURG'S SYNDROME AND HETEROCHROMIA IRIDUM IN A DEAF SCHOOL POPULATION.
  • M. Partington
  • Canadian Medical Association journal
  • 1964
  • Corpus ID: 45127013
Waardenburg's syndrome consists of lateral displacement of the inner canthi of the eyes (dystopia canthorum), a broad nasal root… 
1949
1949
Clinical study of lepromatous leprosy in Costa Rica.
Although knowledge of the symptomatology of leprosy is very complete, we believe it of interest to describe the clinical picture…