X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (552) 552
Book Review (68) 68
Publication (41) 41
Book / eBook (12) 12
Conference Proceeding (3) 3
Book Chapter (2) 2
Dissertation (2) 2
Newspaper Article (2) 2
Presentation (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (516) 516
humans (505) 505
genetics & heredity (247) 247
female (245) 245
male (242) 242
chromosome mapping (179) 179
adult (119) 119
middle aged (100) 100
genetics (98) 98
animals (95) 95
gene (95) 95
genetic aspects (87) 87
chromosomes, human, pair 2 - genetics (86) 86
genes (86) 86
in situ hybridization, fluorescence (85) 85
pedigree (85) 85
chromosome aberrations (83) 83
genetic linkage (82) 82
chromosomes, human, pair 2 (76) 76
oncology (76) 76
aged (74) 74
chromosomes (74) 74
linkage (73) 73
mutation (71) 71
mice (66) 66
molecular sequence data (65) 65
karyotyping (64) 64
lod score (63) 63
phenotype (60) 60
genetic predisposition to disease (59) 59
neurosciences (57) 57
analysis (55) 55
biochemistry & molecular biology (55) 55
expression (55) 55
research (55) 55
translocation, genetic (53) 53
adolescent (52) 52
base sequence (52) 52
cell biology (52) 52
child (52) 52
linkage analysis (52) 52
clinical neurology (50) 50
association (49) 49
cancer (49) 49
genotype (46) 46
mutations (46) 46
genetic markers (45) 45
chromosome banding (44) 44
parkinson disease - genetics (44) 44
comparative genomic hybridization (42) 42
amino acid sequence (41) 41
identification (41) 41
disease (40) 40
genomics (38) 38
cytogenetics (37) 37
gene expression (37) 37
locus (37) 37
genome, human (35) 35
haplotypes (35) 35
dna mutational analysis (34) 34
protein (34) 34
alleles (33) 33
child, preschool (33) 33
chromosome 2 (33) 33
genetic predisposition to disease - genetics (33) 33
genetic research (32) 32
polymerase chain reaction (31) 31
pregnancy (31) 31
tumors (31) 31
biotechnology & applied microbiology (30) 30
genomes (30) 30
muscular dystrophies - genetics (30) 30
age of onset (29) 29
aged, 80 and over (28) 28
family health (28) 28
parkinson's disease (28) 28
translocation (28) 28
chromosome deletion (27) 27
cleft lip - genetics (27) 27
dna (27) 27
localization (27) 27
cloning, molecular (26) 26
human genetics (26) 26
polymorphism, single nucleotide (26) 26
proteins (26) 26
alpha-synuclein (25) 25
cleft palate - genetics (25) 25
microsatellite repeats (25) 25
psychiatry (25) 25
genetic linkage - genetics (24) 24
hematology (24) 24
cloning (23) 23
cytogenetic analysis (23) 23
diagnosis (23) 23
genetic testing (23) 23
in-situ hybridization (23) 23
tumor cells, cultured (23) 23
gene amplification (22) 22
hybridization (22) 22
chromosome 2p13 (21) 21
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Genetics, ISSN 1061-4036, 1998, Volume 18, Issue 3, pp. 262 - 265
Parkinson's disease (PD) is a common degenerative neurologic disorder, which is pathologically characterized by a selective degeneration of dopaminergic... 
GENETIC-LINKAGE | HUMAN GENOME | AUTOSOMAL-DOMINANT PARKINSONISM | LEWY BODY | GENETICS & HEREDITY | LINKAGE ANALYSIS | INHERITANCE | Haplotypes | Disease Susceptibility | Humans | Middle Aged | Male | Genetic Markers | Parkinson Disease - genetics | Lod Score | Chromosomes, Human, Pair 2 | Genes, Dominant | Pedigree | Age of Onset | Aged, 80 and over | Adult | Female | Aged | Genetic Linkage
Journal Article
Human Genetics, ISSN 0340-6717, 2004, Volume 96, Issue 1, pp. 99 - 101
It has been previously shown that some toxic effects of high concentrations of glucose are mediated by the hexosamine biosynthesis pathway and its... 
Chromosomes, Human, Pair 2 - genetics | Animals | In Situ Hybridization | Gene Expression - genetics | Humans | RNA, Messenger - genetics | Rats | Glutamine-Fructose-6-Phosphate Transaminase (Isomerizing) - genetics | Index Medicus
Journal Article
Journal Article
Annals of Neurology, ISSN 0364-5134, 1999, Volume 46, Issue 3, pp. 399 - 404
Welander distal myopathy (WDM) is an autosomal dominant myopathy with late-adult onset characterized by slow progression of distal muscle weakness. The... 
SKELETAL-MUSCLE | LOCALIZATION | MIYOSHI-MYOPATHY | GROWTH-FACTOR-ALPHA | INVOLVEMENT | GIRDLE MUSCULAR-DYSTROPHY | LOCUS | MAP | NEUROSCIENCES | LGMD2B | CLINICAL NEUROLOGY | REGION | Haplotypes | Chromosomes, Human, Pair 2 - genetics | Pedigree | Humans | Female | Genotype | Male | Genetic Linkage - genetics | Muscular Diseases - genetics | Lod Score | Index Medicus
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2001, Volume 9, Issue 9, pp. 659 - 666
Parkinson's disease (PD) is a common neurodegenerative disorder with clinical features of bradykinesia, rigidity, resting tremor and postural instability... 
Chromosome 2p13 | Parkinson's disease | Genetic and physical mapping | PARK3 | chromosome 2p13 | LOCALIZATION | PROTEIN | DEMENTIA | BIOCHEMISTRY & MOLECULAR BIOLOGY | genetic and physical mapping | ALPHA-SYNUCLEIN | FAMILY | CLONING | DNA | GENETICS & HEREDITY | INHERITANCE | EXPRESSION | PARKINSONS-DISEASE | Haplotypes | RNA-Binding Proteins - genetics | Microtubule-Associated Proteins - genetics | Humans | DNA, Complementary - genetics | Family Health | Male | Receptors, Retinoic Acid - genetics | Alcohol Oxidoreductases - genetics | Proteins | Chromosomes, Human, Pair 2 - genetics | Protein Tyrosine Phosphatases - genetics | Female | T-Cell Intracellular Antigen-1 | Nuclear Proteins - genetics | Microsatellite Repeats | Poly(A)-Binding Proteins | Genetic Predisposition to Disease - genetics | Early Growth Response Transcription Factors | Endosomal Sorting Complexes Required for Transport | Membrane Proteins - genetics | Dynactin Complex | Genotype | Chromosome Mapping | Parkinson Disease - genetics | Phosphoproteins - genetics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Nerve Tissue Proteins - genetics | Sequence Analysis, DNA | DNA - genetics | alpha-Glucosidases - genetics | Adaptor Proteins, Signal Transducing | DNA - chemistry | Pedigree | Amino Acid Transport Systems - genetics | DNA, Complementary - chemistry | Chaperonins - genetics | Chromosome 19 | Dopamine | Tremor | Neurodegenerative diseases | Cloning | Parkinsons disease | Genomes | Founder effect | Chromosome 2 | Posture | Signal transduction | Genetics | Mutation | Chromosomes | Movement disorders | Deoxyribonucleic acid--DNA | Dementia | Index Medicus
Journal Article
Journal Article
Human Mutation, ISSN 1059-7794, 04/2013, Volume 34, Issue 4, pp. 572 - 577
Journal Article
Journal Article