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Clinical Cancer Research, ISSN 1078-0432, 06/2017, Volume 23, Issue 12, pp. e83 - e90
In October 2016, the American Association for Cancer Research held a meeting of international childhood cancer predisposition syndrome experts to evaluate the... 
GENOTYPE-PHENOTYPE CORRELATION | RUBINSTEIN-TAYBI-SYNDROME | SOTOS-SYNDROME | ONCOLOGY | SCHINZEL-GIEDION-SYNDROME | CAUSE NOONAN | JUVENILE MYELOMONOCYTIC LEUKEMIA | GERM-CELL TUMOR | OF-FUNCTION MUTATIONS | CLINICAL-FEATURES | FACTOR-I TITF-1/NKX2.1 | Abnormalities, Multiple - pathology | Neoplastic Syndromes, Hereditary - pathology | Craniofacial Abnormalities - epidemiology | Sotos Syndrome - epidemiology | Colorectal Neoplasms - genetics | Humans | Brain Neoplasms - pathology | Nails, Malformed - pathology | Intellectual Disability - genetics | Noonan Syndrome - pathology | Neoplastic Syndromes, Hereditary - epidemiology | Rubinstein-Taybi Syndrome - genetics | Congenital Hypothyroidism - genetics | Abnormalities, Multiple - epidemiology | Craniofacial Abnormalities - pathology | Thyroid Nuclear Factor 1 - genetics | Neoplastic Syndromes, Hereditary - genetics | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - genetics | Intellectual Disability - epidemiology | Colorectal Neoplasms - epidemiology | Hand Deformities, Congenital - epidemiology | Sotos Syndrome - genetics | Costello Syndrome - pathology | Sotos Syndrome - pathology | Risk Factors | Intellectual Disability - pathology | Brain Neoplasms - genetics | Rubinstein-Taybi Syndrome - pathology | Noonan Syndrome - genetics | Nails, Malformed - genetics | Costello Syndrome - epidemiology | Costello Syndrome - genetics | Hand Deformities, Congenital - genetics | Nails, Malformed - epidemiology | Rubinstein-Taybi Syndrome - epidemiology | Congenital Hypothyroidism - pathology | Noonan Syndrome - epidemiology | Mutation | Protein Tyrosine Phosphatase, Non-Receptor Type 11 - genetics | Colorectal Neoplasms - pathology | Congenital Hypothyroidism - epidemiology | Hand Deformities, Congenital - pathology | Brain Neoplasms - epidemiology | Brain | Physical examinations | Brain tumors | Health problems | Disorders | Health risks | Aciduria | Risk | Infants | Patients | K-Ras protein | Surveillance | Children | Health risk assessment | Thyroid transcription factor 1 | Metabolic disorders | Cancer
Journal Article
Cerebral Cortex, ISSN 1047-3211, 2000, Volume 10, Issue 10, pp. 981 - 991
Journal Article
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 2013, Volume 69, Issue 4, pp. 625 - 633
Journal Article
British journal of dermatology, ISSN 0007-0963, 2014, Volume 171, Issue 3, pp. 615 - 621
Rubinstein-Taybi syndrome (RSTS) is a multiple congenital anomalies-intellectual disability syndrome. One of the complications is keloid formation. Keloids are... 
MANAGEMENT | MENTAL-RETARDATION | DISEASE | ADULTS | SCALE | HYPERTROPHIC SCARS | DERMATOLOGY | Young Adult | Keloid - pathology | Keloid - etiology | Humans | Age of Onset | Rubinstein-Taybi Syndrome - etiology | Rubinstein-Taybi Syndrome - pathology | Female | Male | Surveys and Questionnaires | Cohort Studies | Clinical trials | Medicine, Experimental | Medical research | Keloids
Journal Article
American journal of medical genetics. Part A, ISSN 1552-4825, 2016, Volume 170, Issue 12, pp. 3069 - 3082
Journal Article
Journal Article
British Journal of Dermatology, ISSN 0007-0963, 09/2014, Volume 171, Issue 3, pp. 452 - 453
Journal Article
Journal Article
NeuroMolecular Medicine, ISSN 1535-1084, 3/2014, Volume 16, Issue 1, pp. 16 - 24
Rubinstein–Taybi syndrome (RTS) is an incurable genetic disorder with combination of mental retardation and physical features including broad thumbs and toes,... 
RTS | CBP | Neurology | Neurosciences | Biomedicine | Histone methylation | Internal Medicine | Histone acetylation | HDAC | LONG-TERM-MEMORY | DNA-DAMAGE | SYNAPTIC PLASTICITY | NEUROSCIENCES | MOLECULAR ANALYSIS | ACETYLTRANSFERASE ACTIVITY | MOUSE MODEL | CREBBP GENE | HISTONE DEACETYLASE INHIBITORS | HUNTINGTONS-DISEASE | CHROMOSOME 16P13.3 | Sequence Deletion | Epigenesis, Genetic | Humans | CREB-Binding Protein - genetics | Rubinstein-Taybi Syndrome - diagnosis | Rubinstein-Taybi Syndrome - genetics | Histone Acetyltransferases - metabolism | Acetylation | CREB-Binding Protein - deficiency | Disease Models, Animal | Chromatin - ultrastructure | Tumor Suppressor Protein p53 - metabolism | Rubinstein-Taybi Syndrome - pathology | CREB-Binding Protein - physiology | p300-CBP Transcription Factors - metabolism | Animals | Histone-Lysine N-Methyltransferase - metabolism | Models, Biological | Histone Deacetylase Inhibitors - pharmacology | Histone Deacetylase Inhibitors - therapeutic use | Protein Processing, Post-Translational | Histones - metabolism | MicroRNAs - physiology | Mutation | Methylation | Gene mutations | Amyloid beta-protein | Histones | Genetic transcription | Binding proteins | Mental illness | Alzheimer's disease | Protein binding | CREB-binding protein | histone methylation | histone acetylation
Journal Article
Journal Article
Journal Article