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Results of search for 'au:"Neumann, L M"'
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Authors
Armbrust, S
Bartsch, O
Beaudry, J S
Becker, M
Cavanaugh, C
Christensen, C
Engel, W
Foerster, M H
Fusch, C
Gerlach, A
Grollmuss, O
Haas, D
Haas, J-P
Haberl, H
Heineking, B
Hennies, H
Holz, F G
Neitzel, H
Neumann, L M
Schulze, I
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Topics
Abnormalities, Multiple
Adolescent
Adult
Aged
Child
Child, Preschool
DNA Mutational Analysis
Fatal Outcome
Female
Gene Deletion
Humans
In Situ Hybridization, Fluorescence
Infant
Karyotyping
Male
Middle Aged
Mutation
complications
genetics
methods
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English
German
Your search returned 14 results.
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1.
A simple exercise for teaching mirror vision skills.
[electronic resource]
by
Neumann, L M
Producer:
19880328
In:
Journal of dental education
vol. 52
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No items available.
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2.
The use of porcelain-fused-to-metal restorations in current dental practice: a survey.
[electronic resource]
by
Neumann, L M
Producer:
19870527
In:
The Journal of prosthetic dentistry
vol. 57
Online resources:
Available from publisher's website
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3.
Long-term continuing education for general dentists.
[electronic resource]
by
Neumann, L M
Beaudry, J S
Producer:
19870831
In:
Journal of dental education
vol. 51
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No items available.
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4.
Validation of the National Board Dental Hygiene Examination.
[electronic resource]
by
Kramer, G A
Neumann, L M
Producer:
20071029
In:
Journal of dental hygiene : JDH
vol. 81
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No items available.
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5.
Dental esthetic satisfaction in adults.
[electronic resource]
by
Neumann, L M
Christensen, C
Cavanaugh, C
Producer:
19890622
In:
Journal of the American Dental Association (1939)
vol. 118
Online resources:
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6.
Unexpected death of a 12 year old boy with monosomy 1p36.
[electronic resource]
by
Neumann, L M
Polster, T
Spantzel, T
Bartsch, O
Producer:
20040720
In:
Genetic counseling (Geneva, Switzerland)
vol. 15
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7.
Spontaneous intracerebral hemorrhage and multiple infarction in Williams-Beuren syndrome.
[electronic resource]
by
Kalbhenn, T
Neumann, L M
Lanksch, W R
Haberl, H
Producer:
20040224
In:
Pediatric neurosurgery
vol. 39
Online resources:
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8.
Prenatal diagnosis of Alagille syndrome.
[electronic resource]
by
Witt, H
Neumann, L M
Grollmuss, O
Luck, W
Becker, M
Producer:
20040722
In:
Journal of pediatric gastroenterology and nutrition
vol. 38
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9.
Novel mutations in the Atlastin gene (SPG3A) in families with autosomal dominant hereditary spastic paraplegia and evidence for late onset forms of HSP linked to the SPG3A locus.
[electronic resource]
by
Sauter, S M
Engel, W
Neumann, L M
Kunze, J
Neesen, J
Producer:
20040309
In:
Human mutation
vol. 23
Online resources:
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10.
De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probes.
[electronic resource]
by
Tönnies, H
Schulze, I
Hennies, H
Neumann, L M
Keitzer, R
Neitzel, H
Producer:
20020110
In:
Journal of medical genetics
vol. 38
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11.
Molecular cytogenetic identification and characterization of a de novo supernumerary neocentromeric derivative chromosome 13.
[electronic resource]
by
Tonnies, H
Gerlach, A
Heineking, B
Starke, H
Neitzel, H
Neumann, L M
Producer:
20060918
In:
Cytogenetic and genome research
vol. 114
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12.
[Ocular manifestations and surgical results in patients with Marfan syndrome].
[electronic resource]
by
Ladewig, M S
Robinson, P N
Neumann, L M
Holz, F G
Foerster, M H
Producer:
20061128
In:
Der Ophthalmologe : Zeitschrift der Deutschen Ophthalmologischen Gesellschaft
vol. 103
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13.
Smith-Lemli-Opitz syndrome with a classical phenotype, oesophageal achalasia and borderline plasma sterol concentrations.
[electronic resource]
by
Haas, D
Armbrust, S
Haas, J-P
Zschocke, J
Mühlmann, K
Fusch, C
Neumann, L M
Producer:
20060705
In:
Journal of inherited metabolic disease
vol. 28
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14.
A complex phenotype with cystic renal disease.
[electronic resource]
by
Müller, D
Klopocki, E
Neumann, L M
Mundlos, S
Taupitz, M
Schulze, I
Ropers, H-H
Querfeld, U
Ullmann, R
Producer:
20061114
In:
Kidney international
vol. 70
Online resources:
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