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B. Rautenstrauss

Veröffentlichungen von B. Rautenstrauss zu Rautenstrauss, B. ->
weitere Veröffentlichungen von B. Rautenstrauss:
Regional localization of rat peripheral myelin protein 22 (Pmp22) gene to Chromosome 10q22 by FISH (1995)
Accumulation of peripheral myelin protein 22 (PMP22) in onion bulbs of nerves biopsied from patients with different subtypes of Charcot-Marie-Tooth disease type 1 (1997)
Molecular diagnosis of PMP22-associated neuropathies using fluorescence in situ hybridization (FISH) on archival peripheral nerve tissue preparations (1997)
Regional localization of Flic1, a calcyclin/S100A6-like gene, to rat Chromosome 7q22-31 by means of FISH (1998)
Regional localization of rat myelin protein zero Mpz gene to Chromosome 13q24-25 by means of FISH (1995)
Regional localization of rat microvascular endothelial differentiation gene 1 (Mdg1) to Chromosome 6q16-23 by means of FISH (1996)
The Tage4 gene maps to rat Chromosome 1q22 (1997)
Mapping of two different alpha-1,2-fucosyltransferase genes to rat Chromosome 1q22-q31 (1997)
Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: a SacI polymorphism in the proximal CMT1A-REP elements may lead to genetic misdiagnosis (1998)
Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field (1999)
Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversion (1996)
Juvenile open angle glaucoma: fine mapping of the TIGR gene to 1q24.3–q25.2 and mutation analysis (1998)
Charcot-Marie-Tooth disease and related peripheral neuropathies: novel mutations in the peripheral myelin genes connexin 32 (Cx32 ), peripheral myelin protein 22 (PMP22 ), and peripheral myelin protein zero (MPZ ) (2000)
PMP22 Thr118Met is not a clinically relevant CMT1 marker (2000)
Fourth metting of the European Neurological Society 25–29 June 1994 Barcelona, Spain (1994)
Veröffentlichungen zu Rautenstrauss, B.
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1
Liehr, T., Rautenstrauss, B. Regional localization of rat peripheral myelin protein 22 (Pmp22) gene to Chromosome 10q22 by FISH
in: Mammalian genome , ISSN 1432-1777, Vol. 6 (7. 1995), p. 489-489
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1995
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2
Liehr, Thomas, Grehl, Holger, ... Accumulation of peripheral myelin protein 22 (PMP22) in onion bulbs of nerves biopsied from patients with different subtypes of Charcot-Marie-Tooth disease type 1
in: Acta neuropathologica , ISSN 1432-0533, Vol. 94 (5. 1997), p. 514-516
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1997
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3
Liehr, Thomas, Grehl, Holger, ... Molecular diagnosis of PMP22-associated neuropathies using fluorescence in situ hybridization (FISH) on archival peripheral nerve tissue preparations
in: Acta neuropathologica , ISSN 1432-0533, Vol. 94 (3. 1997), p. 266-271
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1997
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4
Pröls, F., Liehr, T., ... Regional localization of Flic1, a calcyclin/S100A6-like gene, to rat Chromosome 7q22-31 by means of FISH
in: Mammalian genome , ISSN 1432-1777, Vol. 9 (1. 1998), p. B094
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1998
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5
Liehr, T., Ekici, A., ... Regional localization of rat myelin protein zero Mpz gene to Chromosome 13q24-25 by means of FISH
in: Mammalian genome , ISSN 1432-1777, Vol. 6 (11. 1995), p. 824-825
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1995
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6
Pröls, F., Liehr, T., ... Regional localization of rat microvascular endothelial differentiation gene 1 (Mdg1) to Chromosome 6q16-23 by means of FISH
in: Mammalian genome , ISSN 1432-1777, Vol. 7 (11. 1996), p. B867
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1996
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7
Chadéneau, C., Liehr, T., ... The Tage4 gene maps to rat Chromosome 1q22
in: Mammalian genome , ISSN 1432-1777, Vol. 8 (2. 1997), p. B157
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1997
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8
Liehr, T., Hallouin, F., ... Mapping of two different alpha-1,2-fucosyltransferase genes to rat Chromosome 1q22-q31
in: Mammalian genome , ISSN 1432-1777, Vol. 8 (4. 1997), p. 297 -298
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1997
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9
Fuchs, Christina, Liehr, Thomas, ... Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: a SacI polymorphism in the proximal CMT1A-REP elements may lead to genetic...
in: Neurogenetics , ISSN 1364-6753, Vol. 2 (1. 1998), p. 43-46
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1998
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10
Nelis, E., Timmerman, V., ... Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving field
in: Neurogenetics , ISSN 1364-6753, Vol. 2 (3. 1999), p. 137-148
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1999
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11
Liehr, T., Rautenstrauss, B., ... Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversion
in: Human genetics , ISSN 1432-1203, Vol. 98 (1. 1996), p. 22-28
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1996
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12
Michels-Rautenstrauss, Karin G., Mardin, Christian Y., ... Juvenile open angle glaucoma: fine mapping of the TIGR gene to 1q24.3–q25.2 and mutation analysis
in: Human genetics , ISSN 1432-1203, Vol. 102 (1. 1998), p. 103-106
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1998
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13
Ekici, A. B., Schweitzer, D., ... Charcot-Marie-Tooth disease and related peripheral neuropathies: novel mutations in the peripheral myelin genes connexin 32 (Cx32 ), peripheral myelin protein 22 (PMP22 ),...
in: Neurogenetics , ISSN 1364-6753, Vol. 3 (1. 2000), p. 49-50
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2000
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14
Young, P., Stögbauer, F., ... PMP22 Thr118Met is not a clinically relevant CMT1 marker
in: Journal of neurology , ISSN 1432-1459, Vol. 247 (9. 2000), p. 696-700
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2000
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15
Harms, L., Bock, A., ... Fourth metting of the European Neurological Society 25–29 June 1994 Barcelona, Spain
in: Journal of neurology , ISSN 1432-1459, Vol. 241 (1. 1994), p. 1-164
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1994