X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (7202) 7202
Book Review (1176) 1176
Publication (694) 694
Book Chapter (141) 141
Conference Proceeding (12) 12
Book / eBook (11) 11
Data Set (2) 2
Dissertation (2) 2
Magazine Article (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (6570) 6570
humans (5298) 5298
female (3370) 3370
male (3358) 3358
genes, recessive (3010) 3010
mutation (2652) 2652
genetics & heredity (2103) 2103
animals (1778) 1778
pedigree (1567) 1567
genetic aspects (1459) 1459
adult (1340) 1340
genetics (1294) 1294
child (1186) 1186
phenotype (1155) 1155
adolescent (984) 984
genes (952) 952
research (933) 933
gene (881) 881
child, preschool (865) 865
mutations (855) 855
research article (843) 843
mice (807) 807
medicine (765) 765
proteins (756) 756
analysis (728) 728
multidisciplinary sciences (725) 725
infant (718) 718
autosomal recessive (691) 691
consanguinity (657) 657
disease (652) 652
middle aged (643) 643
molecular sequence data (631) 631
science (630) 630
dna mutational analysis (624) 624
biochemistry & molecular biology (623) 623
syndrome (617) 617
base sequence (600) 600
infant, newborn (595) 595
homozygote (583) 583
gene mutations (572) 572
pediatrics (567) 567
genes, recessive - genetics (562) 562
genotype (560) 560
alleles (544) 544
neurosciences (540) 540
chromosome mapping (536) 536
cell biology (516) 516
human genetics (478) 478
genetic disorders (467) 467
article (459) 459
genetic linkage (457) 457
clinical genetics (454) 454
biology (451) 451
clinical neurology (449) 449
diagnosis (446) 446
mutation - genetics (446) 446
amino acid sequence (431) 431
gene expression (431) 431
genes, dominant (424) 424
health aspects (422) 422
identification (421) 421
expression (420) 420
genetic research (412) 412
heterozygote (410) 410
genomics (398) 398
abridged index medicus (394) 394
physiological aspects (378) 378
patients (363) 363
protein (363) 363
family (357) 357
abnormalities, multiple - genetics (350) 350
risk factors (350) 350
life sciences (334) 334
genomes (328) 328
young adult (328) 328
children (310) 310
biochemistry (307) 307
genetic predisposition to disease (306) 306
aged (300) 300
biology and life sciences (300) 300
pregnancy (298) 298
dna (287) 287
mutation, missense (286) 286
medicine and health sciences (284) 284
deoxyribonucleic acid--dna (278) 278
disease models, animal (267) 267
dermatology (265) 265
genetic testing (263) 263
neurology (263) 263
medical research (262) 262
polymerase chain reaction (253) 253
sequence analysis, dna (251) 251
ophthalmology (249) 249
haplotypes (245) 245
deafness (241) 241
molecular biology (241) 241
care and treatment (234) 234
cystic fibrosis (232) 232
enzymes (231) 231
medicine, research & experimental (230) 230
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (7220) 7220
French (30) 30
German (23) 23
Russian (17) 17
Japanese (6) 6
Dutch (5) 5
Spanish (4) 4
Chinese (2) 2
Polish (2) 2
Afrikaans (1) 1
Hungarian (1) 1
Italian (1) 1
Norwegian (1) 1
Portuguese (1) 1
Serbian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Movement Disorders, ISSN 0885-3185, 03/2012, Volume 27, Issue 3, pp. 442 - 446
Journal Article
Journal of Community Genetics, ISSN 1868-310X, 7/2016, Volume 7, Issue 3, pp. 215 - 228
Populations practising customary consanguineous marriage have a higher incidence of autosomal recessive genetic disorders than those in which reproductive... 
Human Genetics | Gene Function | Public Health | Biomedicine | Gene Therapy | Ethnic health inequalities | Cousin marriage | Autosomal recessive genetic conditions | Formative service review | Consanguinity | Epidemiology | Genetic disorders | Research | Health aspects | Risk factors | Original
Journal Article
Neurogenetics, ISSN 1364-6745, 11/2006, Volume 7, Issue 4, pp. 231 - 237
The aim of this study was to estimate familial risks of Parkinson’s disease (PD) in first-degree relatives of probands with PD compared with first-degree... 
Human Genetics | Neurosciences | Biomedicine | Familial Parkinson’s disease | Patient admission | Recessive genetic conditions | Molecular Medicine | Heredity | Parkinson’s disease
Journal Article
Journal Article
Journal of Genetic Counseling, ISSN 1059-7700, 4/2016, Volume 25, Issue 2, pp. 359 - 372
Journal Article
Mathematical Biosciences, ISSN 0025-5564, 1991, Volume 104, Issue 1, pp. 97 - 109
A model for carcinogenesis that postulates two rate-limiting events for malignant transformation is a generalization of the recessive oncogenesis hypothesis,... 
Animals | Liver Neoplasms - genetics | Neoplasms - genetics | Cell Transformation, Neoplastic | Humans | Probability | Mathematics | Models, Genetic | Genes, Recessive | Genes, Tumor Suppressor | Precancerous Conditions - genetics | Oncogenes | Index Medicus
Journal Article
Journal Article