Normal view MARC view ISBD view

SPRINT: a tool for probabilistic source term prediction for use with decision support systems. [electronic resource]

By:

Grindon, E

Contributor(s):

Kinniburgh, C G

Producer: 20050127Description: 35-9 p. digitalISSN:

0144-8420

Subject(s):

Online resources:

Available from publisher's website

In: Radiation protection dosimetry vol. 109

Tags from this library: No tags from this library for this title. Log in to add tags.

Average rating: 0.0 (0 votes)

No physical items for this record

Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review

There are no comments on this title.

to post a comment.

Back to results

1 [DNA diagnosis of muscular dystrophies].
by Lindlöf, M
2 Linked polymorphic DNA markers in the prediction of X-linked muscular dystrophy.
by Lindlöf, M
3 Notable losses at specific regions of chromosomes 10q and 13q in the Sézary syndrome detected by comparative genomic hybridization.
by Karenko, L
4 Carrier testing of children for two X-linked diseases: A retrospective study of comprehension of the test results and social and psychological significance of the testing.
by Järvinen, O
5 Karyotype and BCR studies after bone marrow transplantation for chronic myeloid leukaemia.
by Ruutu, T
6 Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial results.
by Kääriäinen, H
7 Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.
by Lindlöf, M
8 Carrier testing of children for two X-linked diseases: a retrospective evaluation of experience and satisfaction of subjects and their mothers.
by Järvinen, O
9 Lymphocytic beta-adrenergic receptors in X-linked muscular dystrophy.
by Mäki, T
10 Microdeletions in patients with X-linked muscular dystrophy: molecular-clinical correlations.
by Lindlöf, M
11 Norrie disease caused by a gene deletion allowing carrier detection and prenatal diagnosis.
by de la Chapelle, A
12 Combined RT-PCR and metaphase-FISH posttransplant studies in pediatric patients with chronic myeloid leukemia.
by Vettenranta, K
13 Philadelphia chromosome as the sole abnormality and p210 bcr-abl chimeric protein expression in an Epstein-Barr virus-transformed B cell line from a patient with chronic myeloid leukemia.
by Knuutila, S
14 Carrier testing of children for two X linked diseases in a family based setting: a retrospective long term psychosocial evaluation.
by Järvinen, O
15 [Diagnosis of Duchenne's muscular dystrophy using recombinant DNA technics].
by Lindlöf, M
16 Erythropoietin receptor mutations associated with familial erythrocytosis cause hypersensitivity to erythropoietin in the heterozygous state.
by Watowich, S S
17 Coincident maternal meiotic nondisjunction of chromosomes X and 21 without evidence of autosomal asynapsis.
by Ikonen, R S
18 Prenatal diagnosis of X-linked chronic granulomatous disease using restriction fragment length polymorphism analysis.
by Lindlöf, M
19 Gene deletions in X-linked muscular dystrophy.
by Lindlöf, M
20 Linkage studies in a new X-linked myopathy, suggesting exclusion of DMD locus and tentative assignment to distal Xq.
by Saviranta, P