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Results of search for 'au:"Röhrig, D"'
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Authors
Bathke, K D
Glauner, B
Hahnen, E
Hartig, W
Knapp, M
Koch, M C
Köhler, J
Morgan, G
Nicholson, G
Nicholson, G A
Piechaczek, B
Rudnik-Schöneborn, S
Röhrig, D
Saule, H
Schmidt, W
Schmoz, G
Voosen, B
Wirth, B
Wustmann, M
Zerres, K
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Topics
Adolescent
Adult
Age of Onset
Aged
Child
Chromosomes, Human, Pair 5
Female
Genetic Linkage
Humans
Infant
Male
Middle Aged
Muscular Atrophy, Spinal
Pedigree
Pregnancy
Pregnancy Complications
Retrospective Studies
Spinal Muscular Atrophies of Childhood
etiology
genetics
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English
German
Your search returned 12 results.
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1.
[Suxamethonium-induced hyperkalemia in patients with spinal cord lesions].
[electronic resource]
by
Schmidt, W
Röhrig, D
Producer:
19731116
In:
Zentralblatt fur Neurochirurgie
vol. 33
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2.
Increased risk for abnormal placentation in women affected by myotonic dystrophy.
[electronic resource]
by
Rudnik-Schöneborn, S
Röhrig, D
Zerres, K
Producer:
19981210
In:
Journal of perinatal medicine
vol. 26
Online resources:
Available from publisher's website
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3.
[Amino acid metabolism in post-stress metabolism].
[electronic resource]
by
Wustmann, M
Röhrig, D
Schmoz, G
Hartig, W
Producer:
19840831
In:
Zeitschrift fur experimentelle Chirurgie, Transplantation, und kunstliche Organe : Organ der Sektion Experimentelle Chirurgie der Gesellschaft fur Chirurgie der DDR
vol. 17
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4.
Obstetric aspects in women with facioscapulohumeral muscular dystrophy, limb-girdle muscular dystrophy, and congenital myopathies.
[electronic resource]
by
Rudnik-Schöneborn, S
Glauner, B
Röhrig, D
Zerres, K
Producer:
19970821
In:
Archives of neurology
vol. 54
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5.
[Spinal muscular atrophy in childhood. Possibilities and limits of clinical and molecular genetic diagnosis].
[electronic resource]
by
Zerres, K
Rudnik-Schöneborn, S
Röhrig, D
Wirth, B
Producer:
19940215
In:
Monatsschrift Kinderheilkunde : Organ der Deutschen Gesellschaft fur Kinderheilkunde
vol. 141
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6.
Pregnancy and delivery in Charcot-Marie-Tooth disease type 1.
[electronic resource]
by
Rudnik-Schöneborn, S
Röhrig, D
Nicholson, G
Zerres, K
Producer:
19931112
In:
Neurology
vol. 43
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7.
Evaluation of the facioscapulohumeral muscular dystrophy (FSHD1) phenotype in correlation to the concurrence of 4q35 and 10q26 fragments.
[electronic resource]
by
Köhler, J
Röhrig, D
Bathke, K D
Koch, M C
Producer:
19990601
In:
Clinical genetics
vol. 55
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8.
Exclusion of the gene locus for spinal muscular atrophy on chromosome 5q in a family with infantile olivopontocerebellar atrophy (OPCA) and anterior horn cell degeneration.
[electronic resource]
by
Rudnik-Schöneborn, S
Wirth, B
Röhrig, D
Saule, H
Zerres, K
Producer:
19950522
In:
Neuromuscular disorders : NMD
vol. 5
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9.
Autosomal recessive proximal spinal muscular atrophy in 101 sibs out of 48 families: clinical picture, influence of gender, and genetic implications.
[electronic resource]
by
Rudnik-Schöneborn, S
Röhrig, D
Morgan, G
Wirth, B
Zerres, K
Producer:
19940808
In:
American journal of medical genetics
vol. 51
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10.
Prenatal prediction in families with autosomal recessive proximal spinal muscular atrophy (5q11.2-q13.3): molecular genetics and clinical experience in 109 cases.
[electronic resource]
by
Wirth, B
Rudnik-Schöneborn, S
Hahnen, E
Röhrig, D
Zerres, K
Producer:
19950921
In:
Prenatal diagnosis
vol. 15
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11.
Different patterns of obstetric complications in myotonic dystrophy in relation to the disease status of the fetus.
[electronic resource]
by
Rudnik-Schöneborn, S
Nicholson, G A
Morgan, G
Röhrig, D
Zerres, K
Producer:
19990217
In:
American journal of medical genetics
vol. 80
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12.
Fine mapping and narrowing of the genetic interval of the spinal muscular atrophy region by linkage studies.
[electronic resource]
by
Wirth, B
Voosen, B
Röhrig, D
Knapp, M
Piechaczek, B
Rudnik-Schöneborn, S
Zerres, K
Producer:
19930316
In:
Genomics
vol. 15
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