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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.
Highly Cited
2007
Highly Cited
2007
1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features
The 22q11.2 microduplication syndrome is caused by non‐allelic homologous recombination mediated by misalignments of low copy… 
Highly Cited
1999
Highly Cited
1999
Raising eyebrows with botulinum toxin.
BACKGROUND Brow elevation rejuvenates the facial appearance. OBJECTIVE To determine if a significant degree of brow elevation… 
1998
1998
Plastic surgery of the face in Byzantium in the fourth century.
Oribasius was an eminent Byzantine physician who lived in the fourth century. His greatest contribution to medical history was… 
Highly Cited
1995
Highly Cited
1995
Judgment of Gender through Facial Parts
Japanese male and female undergraduate students judged the gender of a variety of facial images. These images were combinations… 
1995
1995
Hereditary hypotrichosis simplex of the scalp.
We report on a female aged 13 years, whose scalp hair began to disappear at the age of 9 years, leaving only sparse wispy hairs… 
1994
1994
Evidence for genetic homogeneity of Setleis' syndrome and focal facial dermal dysplasia
Summary A healthy 14‐month‐old boy had multiple, circular, scar‐like depressions on both temples, which had been present since… 
Review
1989
Review
1989
Duplication 7p de novo and literature review.
We report on a boy with duplication of the short arm of chromosome 7 (karyotype 46,XY, dup (7) (p11.2----pter), QFQ, GTG, RBA… 
1981
1981
Ring chromosome 14: a distinct clinical entity.
An infant girl with ring chromosome 14 is presented. The findings in this patient and in six previously reported cases of a ring… 
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… 
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… 
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