X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (2548) 2548
Publication (202) 202
Book Chapter (55) 55
Newsletter (40) 40
Book Review (26) 26
Conference Proceeding (3) 3
Book / eBook (2) 2
Newspaper Article (2) 2
Web Resource (2) 2
Magazine Article (1) 1
Reference (1) 1
Streaming Video (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (2021) 2021
female (1097) 1097
male (1007) 1007
index medicus (880) 880
hamartoma (695) 695
adult (636) 636
hamartoma - pathology (521) 521
hamartoma syndrome, multiple - genetics (448) 448
child (443) 443
middle aged (441) 441
surgery (360) 360
diagnosis, differential (341) 341
adolescent (335) 335
pathology (326) 326
pediatrics (310) 310
child, preschool (304) 304
infant (286) 286
mutation (284) 284
tumors (282) 282
hamartoma - diagnosis (276) 276
diagnosis (271) 271
dermatology (268) 268
magnetic resonance imaging (265) 265
pten phosphohydrolase - genetics (246) 246
cancer (243) 243
hamartoma - complications (240) 240
oncology (238) 238
clinical neurology (233) 233
hamartoma syndrome, multiple - pathology (232) 232
genetics & heredity (229) 229
hamartoma - surgery (212) 212
hamartoma syndrome, multiple - diagnosis (212) 212
pten (202) 202
cowden syndrome (201) 201
syndrome (195) 195
aged (194) 194
skin neoplasms - pathology (183) 183
research (182) 182
disease (179) 179
medicine & public health (177) 177
genetic aspects (174) 174
gene (165) 165
care and treatment (161) 161
infant, newborn (160) 160
germ-line mutation (158) 158
hamartoma syndrome, multiple - complications (146) 146
children (143) 143
tomography, x-ray computed (142) 142
immunohistochemistry (140) 140
case report (133) 133
multiple hamartoma syndrome (128) 128
hamartoma - genetics (127) 127
pten phosphohydrolase (125) 125
risk factors (119) 119
radiology, nuclear medicine & medical imaging (118) 118
germline mutations (115) 115
health aspects (113) 113
treatment outcome (110) 110
epilepsy (108) 108
hypothalamic hamartoma (108) 108
mutations (107) 107
gastroenterology & hepatology (106) 106
tuberous sclerosis (105) 105
cowden-syndrome (104) 104
case studies (103) 103
animals (101) 101
phenotype (101) 101
pedigree (99) 99
young adult (97) 97
biopsy (96) 96
hamartomas (96) 96
skin (94) 94
neurosciences (93) 93
phosphoric monoester hydrolases - genetics (93) 93
riley-ruvalcaba-syndrome (92) 92
gene mutations (91) 91
tumor suppressor proteins - genetics (90) 90
genetic predisposition to disease (89) 89
tumor suppressor proteins (89) 89
follow-up studies (86) 86
hamartoma - diagnostic imaging (85) 85
lhermitte-duclos disease (81) 81
ophthalmology (81) 81
article (80) 80
congenital, hereditary, and neonatal diseases and abnormalities (80) 80
genetics (80) 80
seizures (75) 75
expression (74) 74
skin diseases - pathology (74) 74
analysis (72) 72
breast neoplasms - genetics (72) 72
peutz-jeghers syndrome - genetics (72) 72
retrospective studies (72) 72
peutz-jeghers syndrome (71) 71
abridged index medicus (70) 70
skin neoplasms - genetics (70) 70
tumor (69) 69
breast cancer (67) 67
breast-cancer (67) 67
breast (66) 66
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (2474) 2474
French (60) 60
German (43) 43
Japanese (21) 21
Spanish (16) 16
Korean (7) 7
Dutch (5) 5
Turkish (4) 4
Portuguese (3) 3
Chinese (2) 2
Czech (2) 2
Arabic (1) 1
Danish (1) 1
Hungarian (1) 1
Italian (1) 1
Russian (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


2015, ISBN 0444627022, Volume 132
PTEN hamartoma tumor syndrome (PHTS) is the molecular diagnostic term describing patients with Cowden syndrome, Bannayan–Riley–Ruvalcaba syndrome, and other... 
Cowden syndrome | Cancer genetics | surveillance | management | PTEN hamartoma tumor syndrome | Bannayan–Riley–Ruvalcaba syndrome | Management | Surveillance | Bannayan-Riley-Ruvalcaba syndrome | PTEN Phosphohydrolase - genetics | Phenotype | Hamartoma Syndrome, Multiple - genetics | Germ-Line Mutation - genetics | Mutation - genetics | Humans
Book Chapter
Journal Article
Journal Article
Journal Article