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Claes Wadelius

Veröffentlichungen von Claes Wadelius zu Wadelius, Claes ->
weitere Veröffentlichungen von Claes Wadelius:
Molecular studies of haemophilia B in Sweden (1988)
Fine mapping of the gene for autosomal dominant juvenile-onset glaucoma with iridogoniodysgenesis in 6p25-tel (1997)
A missense mutation in the FALDH gene identified in Sjögren-Larsson syndrome patients originating from the northern part of Sweden (1997)
Confirmation of linkage to 1q21-31 in a Danish autosomal dominant juvenile-onset glaucoma family and evidence of genetic heterogeneity (1995)
Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysis (1993)
The Sjögren-Larsson Syndrome gene is close to D17S805 as determined by linkage analysis and allelic association (1994)
Refined genetic localization of the Best disease gene in 11q13 and physical mapping of linked markers on radiation hybrids (1997)
The mutation spectrum of the bestrophin protein – functional implications (1999)
Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies (1999)
Identification of the gene responsible for Best macular dystrophy (1998)
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007)
Veröffentlichungen zu Wadelius, Claes
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1
Wadelius, Claes, Blombäck, Margareta, ... Molecular studies of haemophilia B in Sweden
in: Human genetics , ISSN 1432-1203, Vol. 81 (1. 1988), p. 13-17
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1988
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2
Graff, C., Jerndal, Tord, ... Fine mapping of the gene for autosomal dominant juvenile-onset glaucoma with iridogoniodysgenesis in 6p25-tel
in: Human genetics , ISSN 1432-1203, Vol. 101 (2. 1997), p. 130-134
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1997
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3
Sillén, A., Jagell, Sten, ... A missense mutation in the FALDH gene identified in Sjögren-Larsson syndrome patients originating from the northern part of Sweden
in: Human genetics , ISSN 1432-1203, Vol. 100 (2. 1997), p. 201-203
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1997
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4
Graff, Caroline, Urbak, Steen F., ... Confirmation of linkage to 1q21-31 in a Danish autosomal dominant juvenile-onset glaucoma family and evidence of genetic heterogeneity
in: Human genetics , ISSN 1432-1203, Vol. 96 (3. 1995), p. 285-289
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1995
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5
Sulisalo, Tuija, 2, Pertti, ... Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysis
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 3, No. 4 (1993), p. 338-341
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1993
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6
Pigg, Maritta, Jagell, Sten, ... The Sjögren-Larsson Syndrome gene is close to D17S805 as determined by linkage analysis and allelic association
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 8, No. 4 (1994), p. 361-364
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1994
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7
Graff, Caroline, Eriksson, Anna, ... Refined genetic localization of the Best disease gene in 11q13 and physical mapping of linked markers on radiation hybrids
in: Human genetics , ISSN 1432-1203, Vol. 101 (3. 1997), p. 263-270
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1997
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8
Bakall, B., Marknell, Towa, ... The mutation spectrum of the bestrophin protein – functional implications
in: Human genetics , ISSN 1432-1203, Vol. 104 (5. 1999), p. 383-389
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1999
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9
Allikmets, R., Seddon, Johanna M., ... Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies
in: Human genetics , ISSN 1432-1203, Vol. 104 (6. 1999), p. 449-453
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1999
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10
Petrukhin, Konstantin, Koisti, Markus J., ... Identification of the gene responsible for Best macular dystrophy
in: Nature genetics . - New York, NY : Nature America, ISSN 1546-1718, Vol. 19, No. 3 (1998), p. 241-247
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1998
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11
Birney, Ewan, Stamatoyannopoulos, John A., ... Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
in: Nature . - London [u.a.] : Nature Publising Group, ISSN 1476-4687, Vol. 447, No. 7146 (2007), p. 799-816
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2007