X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (308) 308
Patent (24) 24
Publication (21) 21
Book Review (8) 8
Book / eBook (7) 7
Newspaper Article (5) 5
Book Chapter (3) 3
Dissertation (2) 2
Conference Proceeding (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (199) 199
humans (197) 197
medical and health sciences (164) 164
medicin och hälsovetenskap (164) 164
female (123) 123
genetics & heredity (120) 120
male (118) 118
medicine (103) 103
medicin (95) 95
mutation (89) 89
pedigree (85) 85
adult (67) 67
child (46) 46
molecular sequence data (44) 44
mutations (39) 39
gene (38) 38
base sequence (37) 37
genetic aspects (35) 35
genetics (35) 35
middle aged (35) 35
phenotype (35) 35
biochemistry & molecular biology (34) 34
basic medicine (30) 30
chromosome mapping (30) 30
dna mutational analysis (30) 30
medical genetics (30) 30
medicinska och farmaceutiska grundvetenskaper (30) 30
medicinsk genetik (29) 29
clinical medicine (28) 28
klinisk medicin (28) 28
genes (27) 27
research (27) 27
adolescent (26) 26
expression (26) 26
child, preschool (25) 25
infant (25) 25
animals (24) 24
genetic linkage (24) 24
heterozygote (24) 24
amino acid sequence (23) 23
chemistry (22) 22
genotype (22) 22
aged (21) 21
biochemistry (21) 21
gene mutations (21) 21
haplotypes (21) 21
proteins (21) 21
hematology (20) 20
article (19) 19
beer (19) 19
enzymology (19) 19
genetic predisposition to disease (19) 19
identification (19) 19
metallurgy (19) 19
microbiology (19) 19
mutation or genetic engineering (19) 19
mutation, missense (19) 19
spirits (19) 19
vinegar (19) 19
wine (19) 19
analysis (18) 18
family (18) 18
linkage (18) 18
ribosomal proteins - genetics (18) 18
mice (17) 17
research article (17) 17
anemia, diamond-blackfan - genetics (16) 16
disease (16) 16
polymorphism, single nucleotide (16) 16
risk factors (16) 16
sweden (16) 16
syndrome (16) 16
x chromosome (16) 16
compositions thereof (15) 15
culture media (15) 15
diamond-blackfan anemia (15) 15
dna (15) 15
microorganisms or enzymes (15) 15
propagating, preserving or maintaining microorganisms (15) 15
alleles (14) 14
gene deletion (14) 14
gene expression (14) 14
genetic markers (14) 14
locus (14) 14
pregnancy (14) 14
deletion (13) 13
genetic disorders (13) 13
laboratories (13) 13
neurosciences (13) 13
organic chemistry (13) 13
peptides (13) 13
abridged index medicus (12) 12
anemia (12) 12
consanguinity (12) 12
health aspects (12) 12
homozygote (12) 12
human necessities (12) 12
hygiene (12) 12
infant, newborn (12) 12
medical or veterinary science (12) 12
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (336) 336
French (14) 14
German (10) 10
Swedish (8) 8
Danish (4) 4
Norwegian (1) 1
Spanish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Medical Humanities, ISSN 0022-2593, 05/1980, Volume 37, Issue 2, p. 128
ABSTRACT Mobilisation of mercury by thiol-complexing agents is the accepted treatment for chronic mercury intoxication. The success of such treatment is judged... 
Journal Article
1987, Scandinavian library., ISBN 8200184900, 195
Book
Genomics, ISSN 0888-7543, 1988, Volume 3, Issue 4, pp. 296 - 298
A MspI polymorphism was detected in the β-glucocerebrosidase gene in 10 Swedish families affected by type III Gaucher's disease. The sizes of the polymorphic... 
Journal Article
Archives of Ophthalmology, ISSN 0003-9950, 10/1988, Volume 106, Issue 10, pp. 1414 - 1416
• Diagnosis of X-linked juvenile retinoschisis (RS) was made in two nonrelated Swedish individuals with restriction fragment length polymorphisms, using probes... 
Electroretinography | Haplotypes | DNA Probes | Retinal Diseases - genetics | Retinal Diseases - diagnosis | Humans | Infant | Male | Chromosome Mapping | Pregnancy | Pedigree | X Chromosome | Female | Genetic Carrier Screening | Genetic Linkage | Index Medicus | Abridged Index Medicus
Journal Article
Cancer Genetics and Cytogenetics, ISSN 0165-4608, 1990, Volume 46, Issue 1, pp. 115 - 123
Journal Article
Cancer Genetics and Cytogenetics, ISSN 0165-4608, 05/1990, Volume 46, Issue 1, pp. 115 - 123
Journal Article
American Journal of Medical Genetics, ISSN 0148-7299, 1991, Volume 38, Issue 2-3, pp. 322 - 327
A new RFLP marker U6.2 defining the locus DXS304 was recently mapped to the distal long arm of the X chromosome. In the present study we report the results of... 
genetic linkage | DNA markers | RFLPs | TELOMERIC REGION | RECOMBINATION | DIAGNOSIS | MENTAL-RETARDATION | DNA MARKERS | FACTOR-VIII GENE | GENETIC LINKAGE | PROBES | CHROMOSOME | FAMILIES | FREQUENCY | GENETICS & HEREDITY | SEGREGATION ANALYSIS | RFLPS | Fragile X Syndrome - genetics | DNA Probes | Polymorphism, Restriction Fragment Length | Pedigree | Recombination, Genetic | Humans | Female | Male | Risk | Software | Genetic Markers | Lod Score | DNA | loci | Index Medicus
Journal Article
American Journal of Medical Genetics, ISSN 0148-7299, 1991, Volume 38, Issue 2-3, pp. 319 - 321
Journal Article
Clinical Genetics, ISSN 0009-9163, 1992, Volume 42, Issue 4, pp. 214 - 215
The life expectancy for patients with CF is steadily increasing, resulting in more females with CF reaching fertile age. The risk of having an affected fetus... 
LINKAGE DISEQUILIBRIUM | GENETICS & HEREDITY | Gene Frequency | Humans | Risk Factors | Cystic Fibrosis - epidemiology | Sweden - epidemiology | Genetic Counseling | Linkage Disequilibrium | Pregnancy | DNA Mutational Analysis | Pedigree | Cystic Fibrosis - genetics | Adult | Female | Mutation | mutation | man | prenatal diagnosis | cystic fibrosis
Journal Article
American Journal of Medical Genetics, ISSN 0148-7299, 1992, Volume 44, Issue 6, pp. 830 - 833
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.