Rieger syndrome is not associated with PAX6 deletion: a correction to Acta Ophthalmol Scand 2001: 79: 201-203

Ruth Riise; Barbara D'haene; Elfride De Baere; Karen Grønskov; Karen Brøndum-Nielsen

doi:10.1111/j.1755-3768.2009.01696.x

Rieger syndrome is not associated with PAX6 deletion: a correction to Acta Ophthalmol Scand 2001: 79: 201-203

Ruth Riise, Barbara D'haene, Elfride De Baere, Karen Grønskov, Karen Brøndum-Nielsen

Afdeling for Genetik DIA

7 Citationer (Scopus)

Originalsprog	Engelsk
Tidsskrift	Acta Ophthalmologica (Online)
Vol/bind	87
Udgave nummer	8
Sider (fra-til)	923
ISSN	1755-3768
DOI	https://doi.org/10.1111/j.1755-3768.2009.01696.x
Status	Udgivet - nov. 2009

Adgang til dokumentet

10.1111/j.1755-3768.2009.01696.x

Citationsformater

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title = "Rieger syndrome is not associated with PAX6 deletion: a correction to Acta Ophthalmol Scand 2001: 79: 201-203",

keywords = "Abnormalities, Multiple/genetics, Anterior Eye Segment/abnormalities, Eye Abnormalities/genetics, Eye Proteins/genetics, Face/abnormalities, Gene Deletion, Genes, Dominant, Homeodomain Proteins/genetics, Humans, Iris/abnormalities, PAX6 Transcription Factor, Paired Box Transcription Factors/genetics, Repressor Proteins/genetics, Skin Abnormalities, Syndrome, Tooth Abnormalities/genetics",

author = "Ruth Riise and Barbara D'haene and {De Baere}, Elfride and Karen Gr{\o}nskov and Karen Br{\o}ndum-Nielsen",

year = "2009",

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T1 - Rieger syndrome is not associated with PAX6 deletion

T2 - a correction to Acta Ophthalmol Scand 2001: 79: 201-203

AU - Riise, Ruth

AU - D'haene, Barbara

AU - De Baere, Elfride

AU - Grønskov, Karen

AU - Brøndum-Nielsen, Karen

PY - 2009/11

Y1 - 2009/11

KW - Abnormalities, Multiple/genetics

KW - Anterior Eye Segment/abnormalities

KW - Eye Abnormalities/genetics

KW - Eye Proteins/genetics

KW - Face/abnormalities

KW - Gene Deletion

KW - Genes, Dominant

KW - Homeodomain Proteins/genetics

KW - Humans

KW - Iris/abnormalities

KW - PAX6 Transcription Factor

KW - Paired Box Transcription Factors/genetics

KW - Repressor Proteins/genetics

KW - Skin Abnormalities

KW - Syndrome

KW - Tooth Abnormalities/genetics

U2 - 10.1111/j.1755-3768.2009.01696.x

DO - 10.1111/j.1755-3768.2009.01696.x

M3 - Journal article

C2 - 19764918

SN - 1755-3768

VL - 87

SP - 923

JO - Acta Ophthalmologica (Online)

JF - Acta Ophthalmologica (Online)

IS - 8

ER -