X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (121) 121
humans (104) 104
genetics & heredity (55) 55
female (49) 49
male (40) 40
animals (34) 34
molecular sequence data (34) 34
chromosome mapping (32) 32
mutation (30) 30
base sequence (28) 28
article (27) 27
neoplasm proteins - genetics (25) 25
multiple endocrine neoplasia type 1 - genetics (24) 24
gene (23) 23
genes (23) 23
oncology (23) 23
cancer (21) 21
polymerase chain reaction (21) 21
adult (20) 20
proto-oncogene proteins (20) 20
biochemistry & molecular biology (19) 19
genetic markers (19) 19
mice (19) 19
mutations (19) 19
research (18) 18
genetic aspects (17) 17
genetics (17) 17
alleles (16) 16
cloning, molecular (16) 16
pedigree (16) 16
tumors (16) 16
cell biology (15) 15
analysis (14) 14
chromosomes, human, pair 17 (14) 14
genomics (14) 14
middle aged (14) 14
sequence analysis, dna (14) 14
amino acid sequence (13) 13
expression (13) 13
genes, tumor suppressor (13) 13
genetic research (13) 13
chromosomes (12) 12
chromosomes, artificial, yeast (12) 12
chromosomes, human, pair 11 - genetics (12) 12
dna (12) 12
menin (12) 12
multidisciplinary sciences (12) 12
parathyroid tumors (12) 12
protein (12) 12
abridged index medicus (11) 11
breast neoplasms - genetics (11) 11
congenital, hereditary, and neonatal diseases and abnormalities (11) 11
genetic mapping (11) 11
genomes (11) 11
polymorphism, genetic (11) 11
polymorphism, single nucleotide (11) 11
biochemistry (10) 10
biotechnology & applied microbiology (10) 10
cloning (10) 10
endocrine neoplasia type-1 (10) 10
endocrine system diseases (10) 10
exons (10) 10
heterozygote (10) 10
multiple endocrine neoplasia (10) 10
neoplasms (10) 10
transcription (10) 10
cell line (9) 9
chromosomes, human, pair 11 (9) 9
dna primers (9) 9
endocrine system (9) 9
gene deletion (9) 9
gene mutations (9) 9
identification (9) 9
in situ hybridization, fluorescence (9) 9
localization (9) 9
men1 (9) 9
microbiology (9) 9
neoplasm proteins - metabolism (9) 9
peptides (9) 9
zebrafish (9) 9
aged (8) 8
agriculture (8) 8
anemia (8) 8
animal husbandry (8) 8
beer (8) 8
care of birds, fishes, insects (8) 8
chemistry (8) 8
compositions or test papers therefor (8) 8
compositions thereof (8) 8
condition-responsive control in microbiological orenzymological processes (8) 8
culture media (8) 8
deletion (8) 8
dna sequencing (8) 8
endocrinology & metabolism (8) 8
enzymology (8) 8
fishing (8) 8
forestry (8) 8
hereditary diseases (8) 8
human chromosome 17 (8) 8
human necessities (8) 8
more...
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, 12/2015, Volume 48, Issue 1, pp. 67 - 73
Journal Article
Journal Article
Journal Article
Cell Reports, 07/2015, Volume 12, Issue 1, pp. 35 - 41
Fanconi anemia (FA) is a rare bone marrow failure and cancer predisposition syndrome resulting from pathogenic mutations in genes encoding proteins... 
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 02/2017, Volume 114, Issue 8, pp. 1964 - 1969
Journal Article
Journal of Medical Genetics, ISSN 0022-2593, 06/2017, Volume 54, Issue 6, pp. 417 - 425
Background Diamond-Blackfan anaemia (DBA) is an inherited bone marrow failure syndrome (IBMFS) characterised by erythroid hypoplasia. It is associated with... 
REGULATOR | DIAGNOSIS | MUTATIONS | GENE | GENETICS & HEREDITY | REGISTRY | Complications and side effects | Usage | Ribosomal proteins | Anemia | Causes of | Biosynthesis | Birth defects | Research | Index Medicus
Journal Article
Journal Article
Gastroenterology, ISSN 0016-5085, 2015, Volume 149, Issue 1, pp. 67 - 78
Journal Article
Cancer, ISSN 0008-543X, 10/2017, Volume 123, Issue 20, pp. 3943 - 3954
Patients with Fanconi anemia (FA) are at increased risk of head and neck squamous cell carcinoma (HNSCC), but the prevalence of undiagnosed FA in patients with... 
recessive inherited disorders | Fanconi anemia | head and neck cancers | germline variations | squamous cell carcinoma | VARIANTS | CANCER INCIDENCE | PREVALENCE | ONCOLOGY | FANCD2 | SEQUENCE | SITES | MUTATIONS | DNA-REPAIR | REGISTRY | LIGASE | Fanconi Anemia Complementation Group D2 Protein - genetics | Recombinases - genetics | Carcinoma, Squamous Cell - genetics | Humans | Middle Aged | Fanconi Anemia Complementation Group L Protein - genetics | Fanconi Anemia Complementation Group Proteins - genetics | Fanconi Anemia Complementation Group E Protein - genetics | Male | Sequence Analysis, DNA | Squamous Cell Carcinoma of Head and Neck | DNA Mutational Analysis | Age of Onset | Germ-Line Mutation | Adult | Female | Head and Neck Neoplasms - genetics | Heterozygote | Fanconi Anemia - genetics | High-Throughput Nucleotide Sequencing | Polymorphism, Single Nucleotide | BRCA2 Protein - genetics | Head and neck cancer | Care and treatment | Cancer patients | Genetic aspects | Research | Genetic variation | Genes | Genomes | Mutation rates | DNA repair | Genetic screening | Gene sequencing | Recruitment | Ubiquitination | Clonal deletion | Deletion | Tumorigenesis | Complementation | Neck | Damage | Age | Deoxyribonucleic acid--DNA | Squamous cell carcinoma | Head | Splicing | Cut-off | Anemia | Health risks | Fanconi syndrome | Minority & ethnic groups | Patients | Current carriers | Screening | Sampling methods | Mutation | Cancer | Smoking | Index Medicus | Abridged Index Medicus
Journal Article