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M. Krawczak

Veröffentlichungen von M. Krawczak zu Krawczak, M. ->
weitere Veröffentlichungen von M. Krawczak:
Linkage of the DNA-segment D7S13 (pB79a) with the cystic fibrosis locus (1988)
Molecular reconstruction and homology modelling of the catalytic domain of the common ancestor of the haemostatic vitamin-K-dependent serine proteinases (1996)
Characterization and significance of nine novel mutations in exon 16 of the neurofibromatosis type 1 (NF1) gene (1997)
Recombinant DNA studies of X-linked muscular dystrophies (1986)
Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markers (1987)
Linkage relationship between retinoschisis and four marker loci (1988)
Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families (1988)
Risk of fetal Down's syndrome based on maternal age and varying combinations of maternal serum markers (1994)
Risk of fetal Down's syndrome based on maternal age and varying combinations of maternal serum markers (1994)
A G"+"3-to-T Donor Splice Site Mutation Leads to Skipping of Exon 50 in Von Willebrand Factor mRNA (1994)
Frequency of the cystic fibrosis mutation ΔF508 in Poland (1991)
Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C gene (1992)
Homology modelling of the catalytic domain of early mammalian protein C: evolution of structural features (1997)
Disentangling the perturbational effects of amino acid substitutions in the DNA-binding domain of p53 (1999)
A comparison of methods currently used in clinical practice to estimate familial breast cancer risks (2000)
Veröffentlichungen zu Krawczak, M.
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1
Böhm, D., Krawczak, M., ... Linkage of the DNA-segment D7S13 (pB79a) with the cystic fibrosis locus
in: Human genetics , ISSN 1432-1203, Vol. 78 (2. 1988), p. 186-187
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1988
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2
Krawczak, M., Wacey, Adam, ... Molecular reconstruction and homology modelling of the catalytic domain of the common ancestor of the haemostatic vitamin-K-dependent serine proteinases
in: Human genetics , ISSN 1432-1203, Vol. 98 (3. 1996), p. 351-370
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1996
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3
Maynard, Julie, Krawczak, Michael, ... Characterization and significance of nine novel mutations in exon 16 of the neurofibromatosis type 1 (NF1) gene
in: Human genetics , ISSN 1432-1203, Vol. 99 (5. 1997), p. 674-676
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1997
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4
Wilichowski, E., Krawczak, M., ... Recombinant DNA studies of X-linked muscular dystrophies
in: Fresenius' Zeitschrift für analytische Chemie , ISSN 1618-2650, Vol. 324 (3/4. 1986), p. 272-272
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1986
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5
Wilichowski, E., Krawczak, M., ... Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markers
in: Human genetics , ISSN 1432-1203, Vol. 75 (1. 1987), p. 32-40
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1987
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6
Gellert, G., Petersen, J., ... Linkage relationship between retinoschisis and four marker loci
in: Human genetics , ISSN 1432-1203, Vol. 79 (4. 1988), p. 382-384
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1988
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7
Krawczak, M., Konecki, D. S., ... Allelic association of the cystic fibrosis locus and two DNA markers, XV2c and KM19, in 55 German families
in: Human genetics , ISSN 1432-1203, Vol. 80 (1. 1988), p. 78-80
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1988
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8
Bartels, I., Bockel, B., ... Risk of fetal Down's syndrome based on maternal age and varying combinations of maternal serum markers
in: Archives of gynecology and obstetrics , ISSN 1432-0711, Vol. 255 (2. 1994), p. 57-64
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1994
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9
Bartels, I., Bockel, B., ... Risk of fetal Down's syndrome based on maternal age and varying combinations of maternal serum markers
in: Archives of gynecology and obstetrics , ISSN 1432-0711, Vol. 255 (2. 1994), p. 57-64
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1994
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10
Mertes, G., Ludwig, M., ... A G"+"3-to-T Donor Splice Site Mutation Leads to Skipping of Exon 50 in Von Willebrand Factor mRNA
in: Genomics, in: Genomics . - Amsterdam : Elsevier, ISSN 0888-7543, ZDB-ID 1468023-3 Vol. 24, No. 1 (1994), p. 190-191
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1994
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11
Bal, J., Maciejko, D., ... Frequency of the cystic fibrosis mutation ΔF508 in Poland
in: Human genetics , ISSN 1432-1203, Vol. 86 (3. 1991), p. 329-329
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1991
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12
Grundy, C. B., Schulman, S., ... Protein C deficiency and thromboembolism: recurrent mutation at Arg 306 in the protein C gene
in: Human genetics , ISSN 1432-1203, Vol. 88 (5. 1992), p. 586-588
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1992
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13
Wacey, A. I., Krawczak, M., ... Homology modelling of the catalytic domain of early mammalian protein C: evolution of structural features
in: Human genetics , ISSN 1432-1203, Vol. 101 (1. 1997), p. 37-42
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1997
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14
Wacey, A. I., Cooper, D. N., ... Disentangling the perturbational effects of amino acid substitutions in the DNA-binding domain of p53
in: Human genetics , ISSN 1432-1203, Vol. 104 (1. 1999), p. 15-22
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1999
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15
Tischkowitz, M., Wheeler, D., ... A comparison of methods currently used in clinical practice to estimate familial breast cancer risks
in: Annals of oncology , ISSN 1569-8041, Vol. 11 (4. 2000), p. 451-454
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2000
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16
Zoll, B., Arnemann, J., ... Evidence against close linkage of the loci for fraXq of Martin-Bell syndrome and for factor IX
in: Human genetics , ISSN 1432-1203, Vol. 71 (2. 1985), p. 122-126
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1985
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17
Hecht, W., Pape, B., ... Analysis of the human parathyroid hormone gene region
in: Fresenius' Zeitschrift für analytische Chemie , ISSN 1618-2650, Vol. 324 (3/4. 1986), p. 273-273
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1986
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18
Upadhyaya, M., Ruggieri, M., ... Gross deletions of the neurofibromatosis type 1 (NF1) gene are predominantly of maternal origin and commonly associated with a learning disability, dysmorphic features and...
in: Human genetics , ISSN 1432-1203, Vol. 102 (5. 1998), p. 591-597
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1998
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19
Hallam, Paula J., Wacey, Adam I., ... A novel missense mutation (Thr176→IIe) at the putative hinge of the neo N-terminus of activated protein C
in: Human genetics , ISSN 1432-1203, Vol. 95 (4. 1995), p. 447-450
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1995
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20
Millar, D. S., Steinbrecher, R. A., ... The molecular genetic analysis of haemophilia A; characterization of six partial deletions in the factor VIII gene
in: Human genetics , ISSN 1432-1203, Vol. 86 (2. 1990), p. 219-227
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1990