1.
Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular Protein Transport
by Kolehmainen, Juha
American journal of human genetics, 2003, Vol.72 (6), p.1359-1369
2.
Bardet-Biedl and Cohen syndromes: differential diagnostic criteria
by WARBURG, METTE
Journal of medical genetics, 2000-12, Vol.37 (12), p.e46-46
3.
Delineation of Cohen Syndrome Following a Large-Scale Genotype-Phenotype Screen
by Kolehmainen, Juha
American journal of human genetics, 2004, Vol.75 (1), p.122-127
4.
Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36
by EIBERG, H
Human genetics, 1995, Vol.96 (1), p.33-38
5.
Cytogenetic findings indicate heterogeneity in patients with blepharophimosis, epicanthus inversus, and developmental delay
by Warburg, M
Journal of medical genetics, 1995-01, Vol.32 (1), p.19-24
6.
Duchenne muscular dystrophy: negative electroretinograms and normal dark adaptation. Reappraisal of assignment of X linked incomplete congenital stationary night blindness
by Jensen, H
Journal of medical genetics, 1995-05, Vol.32 (5), p.348-351
7.
Juvenile Kearns-Sayre syndrome initially misdiagnosed as a psychosomatic disorder
by Nørby, S
Journal of medical genetics, 1994-01, Vol.31 (1), p.45-50
8.
X-inactivation pattern in carriers of X-linked retinitis pigmentosa : a valuable means of prognostic evaluation ?
by FRIEDRICH, U
Human genetics, 1993, Vol.92 (4), p.359-363
9.
X-linked retinitis pigmentosa : new map studies of XLRP2, and a possible human centromere effect
by FRIEDRICH, U
Human genetics, 1992, Vol.88 (6), p.683-687
10.
X-LINKED RETINITIS PIGMENTOSA
by Warburg, Mette
The Lancet (British edition), 1967, Vol.290 (7515), p.566-566
11.
Genetics of microphthalmos
by Warburg, M
International ophthalmology, 1981-08, Vol.4 (1-2), p.45-65
12.
Blindness in Mentally Retarded Children. A survey of the causes of blindness in 201 notified patients
by Warburg, M
Documenta ophthalmologica, 1975-12-30, Vol.39 (2), p.343-349
13.
DEVELOPMENT OF THE CORNEA
by Warburg, Mette
The Lancet (British edition), 1974, Vol.303 (7860), p.732-732
14.
Blindness in mentally retarded children: A survey of the causes of blindness in 201 notified patients
by Warburg, Mette
Documenta ophthalmologica, 1975, Vol.39 (1), p.343-349
15.
Dystrophy: a revised definition
by Warburg, M
Journal of medical genetics, 1989-12, Vol.26 (12), p.769-771
16.
Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome
by BLEEKER-WAGEMAKERS, L. M
Human genetics, 1985, Vol.71 (3), p.211-214
17.
X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosome
by FRIEDRICH, U
Human genetics, 1985, Vol.71 (2), p.93-99
18.
Audiological Findings in Norrie's Disease
by Parving, Agnete
Audiology, 1977, Vol.16 (2), p.124-131
19.
A CASE OF SYMMETRICAL MUSCULAR CONTRACTURES DUE TO SARCOIDOSIS
by WARBURG, METTE
Journal of neuropathology and experimental neurology, 1955-07, Vol.14 (3), p.313-315
