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Lancet Oncology, The, ISSN 1470-2045, 2016, Volume 17, Issue 9, pp. 1295 - 1305
Journal Article
Nature Genetics, ISSN 1061-4036, 02/2015, Volume 47, Issue 3, pp. 257 - 262
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 06/2017, Volume 23, Issue 12, pp. e68 - e75
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 06/2017, Volume 23, Issue 12, pp. e76 - e82
Journal Article
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 06/2017, Volume 23, Issue 12, pp. e54 - e61
The neurofibromatoses consist of at least three autosomal-dominant inherited disorders: neurofibromatosis type 1 (NF1), neurofibromatosis type 2 (NF2), and... 
MENINGIOMAS | GENE | ONCOLOGY | SPLICE-SITE MUTATIONS | DISEASE SEVERITY | PRONE SYNDROMES | NF2 | DIAGNOSTIC-CRITERIA | VESTIBULAR-SCHWANNOMA | TYPE-2 NEUROFIBROMATOSIS | FAMILY | Neurofibromin 2 - genetics | Humans | SMARCB1 Protein - genetics | Meningioma - genetics | Neurofibromatoses - genetics | Neurilemmoma - genetics | Meningioma - epidemiology | Skin Neoplasms - diagnosis | Child | Skin Neoplasms - diagnostic imaging | Genetic Predisposition to Disease | Meningioma - diagnostic imaging | Neurofibromatoses - diagnosis | Neurilemmoma - epidemiology | Neurilemmoma - diagnostic imaging | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Skin Neoplasms - epidemiology | Chromosomal Proteins, Non-Histone - genetics | Magnetic Resonance Imaging | Neurofibromatoses - epidemiology | Skin Neoplasms - genetics | Adolescent | Meningioma - diagnosis | Neurofibromin 1 - genetics | Neurofibromatoses - diagnostic imaging | Neurilemmoma - diagnosis | Neuroimaging | Brain | Pediatrics | Central nervous system | Disorders | Neurofibromin 2 | Neurofibromatosis 2 | Nervous system | Malignancy | Risk factors | Vestibular system | Children | Localization | Chromosome 17 | Image resolution | Schwann cells | Recklinghausen's disease | Hereditary diseases | Magnetic resonance imaging | Surveillance | Neurofibromatosis | Chromosome 22 | Meningioma | Tumors | Cancer
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 03/2019, Volume 66, Issue 3, pp. e27546 - n/a
Journal Article
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 2017, Volume 23, Issue 13, pp. e107 - e114
Journal Article
Cancer Research, ISSN 0008-5472, 02/2007, Volume 67, Issue 4, pp. 1415 - 1418
Journal Article
Pediatric Blood & Cancer, ISSN 1545-5009, 01/2018, Volume 65, Issue 1, pp. e26720 - n/a
Journal Article
Clinical Cancer Research, ISSN 1078-0432, 07/2017, Volume 23, Issue 13, pp. e123 - e132
Children and adolescents who present with neuroendocrine tumors are at extremely high likelihood of having an underlying germline predisposition for the... 
PARATHYROID CARCINOMA | PITUITARY-ADENOMA | PRACTICE GUIDELINE | GERM-LINE MUTATIONS | FAMILIAL HYPERPARATHYROIDISM | ONCOLOGY | FUNCTIONAL-CHARACTERIZATION | MEDULLARY-THYROID CARCINOMA | RET PROTOONCOGENE MUTATIONS | TYPE-1 MEN1 | PARAFIBROMIN IMMUNOREACTIVITY | Fibroma - diagnosis | Hyperparathyroidism - diagnosis | Adenoma - epidemiology | Adenoma - genetics | Humans | Multiple Endocrine Neoplasia - genetics | Hyperparathyroidism - epidemiology | Germ-Line Mutation - genetics | Multiple Endocrine Neoplasia - diagnosis | Multiple Endocrine Neoplasia Type 2b - genetics | Jaw Neoplasms - epidemiology | Fibroma - epidemiology | Hyperparathyroidism - genetics | Tumor Suppressor Proteins - genetics | Child | Multiple Endocrine Neoplasia Type 2b - diagnosis | Adenoma - diagnosis | Genetic Predisposition to Disease | Multiple Endocrine Neoplasia - epidemiology | Risk Factors | Proto-Oncogene Proteins - genetics | Fibroma - genetics | Multiple Endocrine Neoplasia Type 2b - epidemiology | Adolescent | Jaw Neoplasms - diagnosis | Jaw Neoplasms - genetics | Proto-Oncogene Proteins c-ret - genetics | Adolescence | Jaw | Disorders | Surveillance | Multiple endocrine neoplasia | Surgery | Genetics | Diagnostic systems | Children | Adolescents | Hyperparathyroidism | Tumors | Cancer | Neuroendocrine tumors | Multiple Endocrine Neoplasia (MEN) 1 | RET | Hyperparathyroid-Jaw Tumor Syndromes | CDKN1B | germline | 2A, 2B, 4 | surveillance | CDC73 | MEN1
Journal Article