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2011, Contemporary neurology series, ISBN 9780199772735, Volume 79., xiv, 482
Book
2011, 1. Aufl., ISBN 1405196262, xxi, 416 p., [4] p. of col. plates
This comprehensive book captures and compiles new and current information on hematologic malignancies. New knowledge of cellular disease processes, molecular... 
Leukemia | Lymphomas | Myelodysplastic syndromes
Book
2011, 2nd ed., ISBN 9781441968203, viii, 204
This practical book is designed to educate physicians and health care workers about the genetic aspects, in the clinical setting, of inherited syndromes of... 
Genetic aspects | Genetic disorders | genetics | Cancer | Neoplastic Syndromes, Hereditary | Neoplastic Syndromes, Hereditary - therapy | Human Genetics | Oncology | Cancer Research | Medicine & Public Health | General Surgery | Surgical Oncology
Book
1974, Annals of the New York Academy of Sciences, Volume 230., 577
Book
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 2013, Volume 68, Issue 2, pp. 189.e1 - 189.e21
Cutaneous findings are not uncommonly a concomitant finding in patients afflicted with gastrointestinal (GI) diseases. The dermatologic manifestations may... 
Cowden syndrome | hereditary and nonhereditary gastrointestinal malignancies | Muir-Torre syndrome | gastrointestinal disorders | hamartomatous polyposis syndrome | Cronkhite-Canada syndrome | Bannayan-Riley-Ruvalcaba syndrome | cutaneous manifestations | Peutz-Jeghers syndrome | Lynch syndrome | paraneoplastic syndrome | PEUTZ-JEGHERS-SYNDROME | RILEY-RUVALCABA-SYNDROME | HEREDITARY COLORECTAL-CANCER | DERMATOLOGY | PERIANAL PAGETS-DISEASE | LESER-TRELAT SIGN | MUIR-TORRE-SYNDROME | NECROLYTIC MIGRATORY ERYTHEMA | FAMILIAL ADENOMATOUS POLYPOSIS | PARANEOPLASTICA BAZEX-SYNDROME | MALIGNANT ACANTHOSIS NIGRICANS | Paraneoplastic Syndromes - genetics | Dermatomyositis - genetics | Carcinoma, Basal Cell - genetics | Colorectal Neoplasms - genetics | Humans | Hypotrichosis - genetics | Gastrointestinal Neoplasms - complications | Acanthosis Nigricans - genetics | Gastrointestinal Neoplasms - pathology | Skin Diseases, Genetic - etiology | Adenomatous Polyposis Coli - genetics | Histiocytoma, Benign Fibrous - genetics | PTEN Phosphohydrolase - genetics | Hamartoma Syndrome, Multiple - genetics | Necrolytic Migratory Erythema - diagnosis | Necrolytic Migratory Erythema - genetics | Intestinal Polyposis - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Malignant Carcinoid Syndrome - genetics | Gastrointestinal Diseases - complications | Peutz-Jeghers Syndrome - genetics | Gastrointestinal Diseases - genetics | Paraneoplastic Syndromes - complications | Hamartoma Syndrome, Multiple - diagnosis | Skin Neoplasms - genetics | Skin Neoplasms - secondary | Colorectal Neoplasms, Hereditary Nonpolyposis - etiology | Mutation
Journal Article
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
Gene, ISSN 0378-1119, 05/2016, Volume 582, Issue 1, pp. 23 - 32
Numerous familial tumor syndromes are associated with distinctive oral mucosal findings, which may make possible an early diagnosis as an efficacious marker... 
Cowden syndrome | Odontogenic keratocystic tumors | Gardner syndrome | Peutz–Jeghers syndrome | Gorlin syndrome | Multiple endocrine neoplasia | Lynch/Muir–Torre syndrome | Ameloblastoma | Familial Adenomatous Polyposis (FAP) | Fordyce granules | Lynch/Muir-Torre syndrome | Peutz-Jeghers syndrome | LYNCH-SYNDROME | NONPOLYPOSIS COLORECTAL-CANCER | PEUTZ-JEGHERS-SYNDROME | COWDEN-DISEASE | Peutz-jeghers syndrome | GARDNERS-SYNDROME | MUIR-TORRE-SYNDROME | BASAL-CELL CARCINOMA | GENETICS & HEREDITY | MUCOCUTANEOUS PIGMENTATION | FAMILIAL ADENOMATOUS POLYPOSIS | Peutz-Jeghers Syndrome - pathology | Humans | Peutz-Jeghers Syndrome - therapy | Muir-Torre Syndrome - therapy | Muir-Torre Syndrome - pathology | Multiple Endocrine Neoplasia - genetics | Germ-Line Mutation - genetics | Molecular Targeted Therapy | Adenomatous Polyposis Coli - pathology | Adenomatous Polyposis Coli - complications | Adenomatous Polyposis Coli - therapy | Adenomatous Polyposis Coli - genetics | Mouth Mucosa - pathology | Gardner Syndrome - pathology | Genes, Tumor Suppressor | Gardner Syndrome - therapy | Gardner Syndrome - complications | Peutz-Jeghers Syndrome - complications | Peutz-Jeghers Syndrome - genetics | Multiple Endocrine Neoplasia - complications | Mouth Mucosa - metabolism | Muir-Torre Syndrome - genetics | Phenotype | Muir-Torre Syndrome - complications | Gardner Syndrome - genetics | Multiple Endocrine Neoplasia - therapy | Heterozygote | Multiple Endocrine Neoplasia - pathology | Genetic aspects | Gene mutations | Cancer
Journal Article
American Journal of Gastroenterology, ISSN 0002-9270, 02/2015, Volume 110, Issue 2, pp. 223 - 262
Journal Article