X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (162) 162
Patent (19) 19
Publication (15) 15
Book Chapter (4) 4
Magazine Article (4) 4
Book / eBook (3) 3
Conference Proceeding (2) 2
Book Review (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (84) 84
genetics & heredity (60) 60
animals (45) 45
female (44) 44
index medicus (44) 44
mice (39) 39
male (37) 37
mutation (31) 31
biochemistry & molecular biology (25) 25
genetic aspects (24) 24
genomic imprinting (24) 24
base sequence (22) 22
molecular sequence data (22) 22
alleles (19) 19
expression (19) 19
chromosome mapping (18) 18
gene expression (18) 18
chemistry (17) 17
genetics (17) 17
dna methylation (16) 16
gene (16) 16
genes (16) 16
metallurgy (16) 16
research (16) 16
analysis (15) 15
cleft palate - genetics (15) 15
gene expression regulation, developmental (15) 15
neural tube defects - genetics (15) 15
compounds thereof (14) 14
inorganic chemistry (14) 14
non-metallic elements (14) 14
sequence analysis, dna (14) 14
syndrome (14) 14
methylation (13) 13
phenotype (13) 13
human necessities (12) 12
hygiene (12) 12
indexing scheme relating to structural and physical aspects ofsolid inorganic compounds (12) 12
medical or veterinary science (12) 12
pregnancy (12) 12
preparations for medical, dental, or toilet purposes (12) 12
specific use of cosmetics or similar toiletpreparations (12) 12
abnormalities, multiple - genetics (11) 11
amino acid sequence (11) 11
article (11) 11
child (11) 11
gene mutations (11) 11
identification (11) 11
mutations (11) 11
adult (10) 10
biotechnology & applied microbiology (10) 10
cell biology (10) 10
chromosomes (9) 9
cleft lip - genetics (9) 9
developmental biology (9) 9
fetus (9) 9
genetic linkage (9) 9
genomics (9) 9
growth (9) 9
medicine (9) 9
pedigree (9) 9
proteins (9) 9
proteins - genetics (9) 9
child, preschool (8) 8
cleft palate (8) 8
dna (8) 8
genomes (8) 8
molecular biology (8) 8
placenta (8) 8
polymerase chain reaction (8) 8
risk factors (8) 8
silver-russell-syndrome (8) 8
cancer (7) 7
deoxyribonucleic acid--dna (7) 7
genetic markers (7) 7
genotype (7) 7
growth disorders - genetics (7) 7
health aspects (7) 7
life sciences (7) 7
loop-tail (7) 7
mice, inbred c57bl (7) 7
mouse (7) 7
neural tube defects (7) 7
polymorphism, genetic (7) 7
reverse transcriptase polymerase chain reaction (7) 7
adolescent (6) 6
articles (6) 6
biology (6) 6
birth weight (6) 6
closure (6) 6
craniofacial development (6) 6
disease models, animal (6) 6
dna - genetics (6) 6
exons (6) 6
family (6) 6
genetic predisposition to disease (6) 6
genetic research (6) 6
grb10 adaptor protein (6) 6
imprinting (6) 6
including grb10 (6) 6
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


Journal Article
Journal Article
Journal of Investigative Dermatology, ISSN 0022-202X, 09/2013, Volume 133, Issue 9, pp. 2229 - 2236
Congenital melanocytic nevi (CMN) can be associated with neurological abnormalities and an increased risk of melanoma. Mutations in , , and have been described... 
MC1R | VARIANTS | RAS | BRAF MUTATIONS | HIGH-FREQUENCY | PHENOTYPE | NEUROLOGICALLY ASYMPTOMATIC CHILDREN | ASSOCIATION | REGISTRY | MOSAICISM | DERMATOLOGY | Meningeal Neoplasms - epidemiology | Prevalence | Nevus, Pigmented - epidemiology | Humans | Child, Preschool | Male | Neurocutaneous Syndromes - congenital | Meningioma - genetics | Mutation, Missense - genetics | Loss of Heterozygosity - genetics | Hamartoma - pathology | Young Adult | Hamartoma - genetics | Nevus, Pigmented - genetics | Meningioma - epidemiology | Zygote | Female | Genetic Predisposition to Disease - epidemiology | Neurocutaneous Syndromes - epidemiology | Child | Melanosis - epidemiology | Melanosis - genetics | Neurocutaneous Syndromes - genetics | Genetic Predisposition to Disease - genetics | Meningeal Neoplasms - genetics | Membrane Proteins - genetics | Central Nervous System Neoplasms - genetics | Risk Factors | Hamartoma - epidemiology | Central Nervous System Neoplasms - epidemiology | Melanosis - congenital | Skin Neoplasms - epidemiology | Nevus, Pigmented - congenital | Magnetic Resonance Imaging | Meningioma - pathology | Central Nervous System Neoplasms - pathology | GTP Phosphohydrolases - genetics | Skin Neoplasms - congenital | Skin Neoplasms - genetics | Adolescent | Mosaicism | Meningeal Neoplasms - pathology | Index Medicus | Original
Journal Article
BMC Medicine, ISSN 1741-7015, 02/2013, Volume 11, Issue 1, pp. 30 - 30
Journal Article
F1000Research, ISSN 2046-1402, 2019, Volume 8, p. 273
Background: Lenz-Majewski syndrome (LMS) is characterized by osteosclerosis and hyperostosis of skull, vertebrae and tubular bones as well as craniofacial,... 
Lecithin | Spine | Homeostasis | Vertebra | Osteoblasts | Defects | Genotype & phenotype | Transfection | Missense mutation | Enzymatic activity | Transgenic animals | Scoliosis | Osteosclerosis | Transgenes | Phosphatidylserine | Majewski syndrome | Enzymes | Phenotypes | Vertebrae | Zebrafish | Ribonucleic acid--RNA | Gene expression | Embryos | Investigations | Chondrocytes | Osteoclasts | Mutation
Journal Article
Journal Article