X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (282) 282
Book Chapter (44) 44
Publication (34) 34
Book / eBook (11) 11
Book Review (9) 9
Conference Proceeding (3) 3
Government Document (2) 2
Reference (1) 1
Trade Publication Article (1) 1
Web Resource (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (167) 167
index medicus (72) 72
genetics & heredity (69) 69
female (66) 66
male (59) 59
child (45) 45
genetics (34) 34
adult (33) 33
child, preschool (32) 32
mutation (31) 31
genomics (30) 30
phenotype (30) 30
adolescent (29) 29
animals (26) 26
neurofibromatosis (26) 26
research (25) 25
article (23) 23
neurofibromatosis 1 - genetics (23) 23
tumors (22) 22
genetic aspects (21) 21
neurofibromatosis 1 - diagnosis (21) 21
nf1 (21) 21
infant (20) 20
pediatrics (19) 19
genetic testing (18) 18
neurofibromatosis type 1 (18) 18
children (17) 17
middle aged (17) 17
gene (16) 16
medical genetics (16) 16
clinical neurology (15) 15
diagnosis (15) 15
genes (15) 15
genetics, medical (15) 15
medicine (15) 15
neurofibromatosis 1 - complications (15) 15
chromosome mapping (13) 13
genetic disorders (13) 13
genomes (13) 13
mutations (13) 13
in situ hybridization, fluorescence (12) 12
medicine, general & internal (12) 12
abnormalities, multiple - genetics (11) 11
oncology (11) 11
risk factors (11) 11
type-1 (11) 11
analysis (10) 10
chromosome aberrations (10) 10
magnetic resonance imaging (10) 10
nerve sheath tumors (10) 10
neurofibromatosis 2 - genetics (10) 10
young adult (10) 10
clinical genetics (9) 9
clinical trials (9) 9
genetic diseases, inborn (9) 9
human genetics (9) 9
infant, newborn (9) 9
mice (9) 9
neurofibromatosis 1 - therapy (9) 9
neurosciences (9) 9
research article (9) 9
syndrome (9) 9
abridged index medicus (8) 8
cancer (8) 8
clinical trials as topic (8) 8
disease (8) 8
expression (8) 8
genetic counseling (8) 8
genetic diseases (8) 8
genetic diseases, inborn - genetics (8) 8
genetics, medical - trends (8) 8
genome, human (8) 8
genotype (8) 8
neurofibromatoses - diagnosis (8) 8
neurofibromatoses - genetics (8) 8
neurofibromin 1 - genetics (8) 8
patients (8) 8
proteins (8) 8
ras (8) 8
studies (8) 8
united states (8) 8
vonrecklinghausen neurofibromatosis (8) 8
care and treatment (7) 7
chromosomes (7) 7
congenital, hereditary, and neonatal diseases and abnormalities (7) 7
diseases (7) 7
dna mutational analysis (7) 7
fish (7) 7
gene deletion (7) 7
genes, neurofibromatosis 1 (7) 7
genetic disease (7) 7
genetic diseases, inborn - diagnosis (7) 7
genetics, medical - education (7) 7
heredity of disease (7) 7
internal medicine (7) 7
karyotyping (7) 7
neurofibromatosis 1 - pathology (7) 7
neurofibromatosis 2 - therapy (7) 7
neurology (7) 7
nf2 (7) 7
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


The American Journal of Human Genetics, ISSN 0002-9297, 01/2018, Volume 102, Issue 1, pp. 3 - 4
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 01/2019, Volume 104, Issue 1, pp. 1 - 3
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 11/2018, Volume 103, Issue 5, pp. 635 - 635
Journal Article
PROTEOMICS, ISSN 1615-9853, 06/2019, Volume 19, Issue 11, pp. e1800334 - n/a
Journal Article
Genetics in Medicine, ISSN 1098-3600, 04/2019, Volume 21, Issue 4, pp. 867 - 876
Neurofibromatosis type 1 (NF1) is characterized by a highly variable clinical presentation, but almost all NF1-affected adults present with cutaneous and/or... 
genotype–phenotype correlation | NF1 | p.Met992del | learning difficulties | neurofibroma | GENETICS & HEREDITY
Journal Article
Journal Article
11/2018, 7, ISBN 9780128125373, 573
For decades, Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics has served as the ultimate resource for clinicians integrating... 
eBook
11/2018, 7, ISBN 0128125365, 414
For decades, Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics has served as the ultimate resource for clinicians integrating... 
Medical genetics
eBook
2007, 5th ed., ISBN 9996004732, 3 v. (xxxix, 3871, xcix p., [30] p. of plates)
Book
Clinical Genetics, ISSN 0009-9163, 05/2015, Volume 87, Issue 5, pp. 399 - 400
Journal Article
Neurology, ISSN 0028-3878, 09/2019, Volume 93, Issue 11, pp. 510 - 514
Journal Article
Clinical Genetics, ISSN 0009-9163, 05/2015, Volume 87, Issue 5, pp. 399 - 400
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 06/2019, Volume 104, Issue 6, pp. 1088 - 1096
Conceptual frameworks are useful in research because they can highlight priority research domains, inform decisions about interventions, identify outcomes and... 
diversity | framework | implementation | genomics | model | translational research | conceptual | Genetic research | Usage | Research | Integrative medicine | Biological diversity
Journal Article
Journal of Child Neurology, ISSN 0883-0738, 1/2018, Volume 33, Issue 1, pp. 82 - 91
Neurofibromatosis type 1 and type 2, affecting both children and adults, often results in devastating complications. The rapid unravelling of the genetic... 
treatment | brain tumor | ophthalmology | genetics | cognition | neuroimaging | PHASE-II | CLINICAL NEUROLOGY | CHILDREN | PLEXIFORM NEUROFIBROMAS | PATHWAY | ADOLESCENTS | MOUSE MODEL | PEDIATRICS | QUALITY-OF-LIFE | TYPE-1 | EXPRESSION | SIROLIMUS
Journal Article
No results were found for your search.

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