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Results of search for 'au:"Preising, M"', page 1 of 2
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Authors
Andrassi, M
Andrassi-Darida, M
Ardjo, S M
Aßmann, C
Baumert, U
Bek, T
Bolz, H J
Bowl, W
Bremser, D
Friedburg, C
Golan, I
Lorenz, B
Müssig, D
Niederdellmann, H
Paunescu, K
Preising, M
Preising, M N
Sitorus, R
Stieger, K
Wagener, H
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Topics
Adolescent
Adult
Child
Child, Preschool
Chloride Channels
DNA Mutational Analysis
Electroretinography
Eye Diseases, Hereditary
Eye Proteins
Female
Genetic Predisposition to Disease
Genetic Testing
Genotype
Humans
Male
Mutation
Phenotype
Retinal Diseases
diagnosis
genetics
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German
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Your search returned 27 results.
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1.
IRPA scientific newsletter--a new website to integrate data on hereditary retinal disorders.
[electronic resource]
by
Preising, M
Lorenz, B
Producer:
19990413
In:
Ophthalmic genetics
vol. 19
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2.
[Framework for qualified inpatient withdrawal treatment of alcoholics in North Rhine-Westphalia].
[electronic resource]
by
Reymann, G
Preising, M
Producer:
20030730
In:
Versicherungsmedizin
vol. 55
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3.
[Albinism and the Range of Fundus Hypopigmentation, Macular Hypoplasia, and Nystagmus].
[electronic resource]
by
Preising, M N
Lorenz, B
Producer:
20161227
In:
Klinische Monatsblatter fur Augenheilkunde
vol. 232
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4.
[Genetic diseases of the retinal pigment epithelium].
[electronic resource]
by
Preising, M N
Lorenz, B
Producer:
20090805
In:
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft
vol. 106
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5.
[Genetics of neuronal ceroidlipofuscinoses. Aspects of genetic counseling].
[electronic resource]
by
Preising, M N
Lorenz, B
Producer:
20101202
In:
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft
vol. 107
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6.
[Best's disease. Overview of pathology and its causes].
[electronic resource]
by
Lorenz, B
Preising, M N
Producer:
20050428
In:
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft
vol. 102
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7.
[Segregation Analysis in Inherited Eye Disorders: An Academic Add-on or An Essential Effort?]
[electronic resource]
by
Preising, M N
Bolz, H J
Producer:
20171113
In:
Klinische Monatsblatter fur Augenheilkunde
vol. 234
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8.
Causes of blindness at the "Wiyata Guna" School for the Blind, Indonesia.
[electronic resource]
by
Sitorus, R
Preising, M
Lorenz, B
Producer:
20031016
In:
The British journal of ophthalmology
vol. 87
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9.
[Erratum: Segregation Analysis in Inherited Eye Disorders: An Academic Add-on or An Essential Effort?]
[electronic resource]
by
Preising, M N
Bolz, H J
Publication details:
Klinische Monatsblatter fur Augenheilkunde
03 2017
In:
Klinische Monatsblatter fur Augenheilkunde
vol. 234
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10.
[Inherited ophthalmological disorders. Part 1: Genetic fundamentals and phenotypes].
[electronic resource]
by
Preising, M N
Stieger, K
Lorenz, B
Producer:
20141105
In:
Klinische Monatsblatter fur Augenheilkunde
vol. 231
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11.
[Inherited ophthalmological disorders. Part 2: Diagnostics and therapeutic concepts].
[electronic resource]
by
Preising, M N
Stieger, K
Lorenz, B
Producer:
20141105
In:
Klinische Monatsblatter fur Augenheilkunde
vol. 231
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12.
Modelling human height and weight: a Bayesian approach towards model comparison.
[electronic resource]
by
Preising, M
Suchomlinov, A
Tutkuviene, J
Aßmann, C
Producer:
20180105
In:
European journal of clinical nutrition
vol. 70
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13.
CYP1B1 gene analysis in primary congenital glaucoma in Indonesian and European patients.
[electronic resource]
by
Sitorus, R
Ardjo, S M
Lorenz, B
Preising, M
Producer:
20030221
In:
Journal of medical genetics
vol. 40
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14.
[Genetic and clinical heterogeneity in LCA patients. The end of uniformity].
[electronic resource]
by
Preising, M N
Paunescu, K
Friedburg, C
Lorenz, B
Producer:
20070926
In:
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft
vol. 104
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15.
Unexpected Genetic Cause in Two Female Siblings with High Myopia and Reduced Visual Acuity.
[electronic resource]
by
Preising, M N
Friedburg, C
Bowl, W
Lorenz, B
Producer:
20181211
In:
BioMed research international
vol. 2018
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16.
Deletion in the OA1 gene in a family with congenital X linked nystagmus.
[electronic resource]
by
Preising, M
Op de Laak, J P
Lorenz, B
Producer:
20010920
In:
The British journal of ophthalmology
vol. 85
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17.
[Recruitment of Suitable Families to Identify Causative Genes in Hereditary Strabismus].
[electronic resource]
by
Preising, M N
Steinmüller, P H T
Lorenz, B
Producer:
20160811
In:
Klinische Monatsblatter fur Augenheilkunde
vol. 232
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18.
An unusual retinal vascular morphology in connection with a novel AIPL1 mutation in Leber's congenital amaurosis.
[electronic resource]
by
Heegaard, S
Rosenberg, T
Preising, M
Prause, J U
Bek, T
Producer:
20030916
In:
The British journal of ophthalmology
vol. 87
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19.
Genotype-phenotype correlation in a German family with a novel complex CRX mutation extending the open reading frame.
[electronic resource]
by
Paunescu, K
Preising, M N
Janke, B
Wissinger, B
Lorenz, B
Producer:
20070731
In:
Ophthalmology
vol. 114
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20.
[Genotype-Phenotype Correlations in Patients with CRB1 Mutations].
[electronic resource]
by
Papadopoulou Laiou, C
Preising, M N
Bolz, H J
Lorenz, B
Producer:
20171113
In:
Klinische Monatsblatter fur Augenheilkunde
vol. 234
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