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Journal Article
Journal of Pediatrics, The, ISSN 0022-3476, 2015, Volume 166, Issue 4, pp. 1048 - 1054.e5
Journal Article
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 01/2015, Volume 23, Issue 3, pp. 292 - 301
Journal Article
Radiographics, ISSN 0271-5333, 09/2011, Volume 31, Issue 5, pp. 1321 - 1340
Journal Article
Journal of the American Academy of Dermatology, ISSN 0190-9622, 11/2011, Volume 65, Issue 5, pp. 893 - 906
There is significant confusion in the literature when describing vascular anomalies, and vascular malformations are often misnamed or incorrectly classified.... 
magnetic resonance | embolization | cutis marmorata telangiectatica congenita | glomuvenous malformation | sclerotherapy | Stewart-Bluefarb syndrome | laser | venous malformation | multi-detector computed tomography | localized intravascular coagulation | pulmonary hypertension vascular malformations | Klippel-Trenaunay syndrome | Parkes Weber syndrome | lymphatic malformation | Macrocephaly-capillary malformation | port-wine stain | surgery | DERMATOLOGY | ARTERIOVENOUS MALFORMATION | VENOUS MALFORMATIONS | KLIPPEL-TRENAUNAY-SYNDROME | BLEB NEVUS SYNDROME | GENUINE DIFFUSE PHLEBECTASIA | CAPILLARY MALFORMATION | ANOMALIES | RILEY-RUVALCABA-SYNDROME | PROTEUS-SYNDROME | MARMORATA-TELANGIECTATICA-CONGENITA | Hemangioma, Capillary - epidemiology | Klippel-Trenaunay-Weber Syndrome - epidemiology | Hemangioma, Capillary - congenital | Humans | Klippel-Trenaunay-Weber Syndrome - diagnosis | Proteus Syndrome - diagnosis | Skin Abnormalities - diagnosis | Vascular Malformations - therapy | Hemangioma, Cavernous - diagnosis | Hemangioma, Capillary - diagnosis | Port-Wine Stain - diagnosis | Adult | Hemangioma, Cavernous - epidemiology | Lymphatic Abnormalities - diagnosis | Child | Infant, Newborn | Hemangioma, Cavernous - congenital | Vascular Malformations - classification | Syndrome | Vascular Malformations - epidemiology | Port-Wine Stain - epidemiology | Algorithms | Glomus Tumor - diagnosis | Leg - blood supply | Vascular Malformations - diagnosis | Hypertrophy | Skin Abnormalities - therapy
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 02/2017, Volume 173, Issue 2, pp. 546 - 549
Baraitser–Winter malformation syndrome (BWMS), Fryns–Aftimos syndrome (FA), and craniofrontofacial syndromes (CFFs) have all been recently proposed to be part... 
ACTB gene | craniofrontofacial syndromes | acute myeloid leukemia | Fryns–Aftimos syndrome | ACTG1 gene | Baraitser–Winter malformation syndrome | Fryns-Aftimos syndrome | FRONTO-FACIAL SYNDROME | CANCER | ACTB | Baraitser-Winter malformation syndrome | RETARDATION | MALFORMATIONS | COLOBOMA | COSTELLO-SYNDROME | GENETICS & HEREDITY | PTOSIS | MUTATIONS | Translocation, Genetic | Lissencephaly - diagnosis | Genetic Testing | Humans | Intellectual Disability - complications | Leukemia, Myeloid, Acute - etiology | Brain - abnormalities | Intellectual Disability - genetics | Young Adult | Facies | Electrocardiography | Leukemia, Myeloid, Acute - drug therapy | Epilepsy - genetics | Female | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - complications | Craniofacial Abnormalities - genetics | Lissencephaly - complications | Treatment Outcome | Bone Marrow Examination | Epilepsy - complications | Epilepsy - diagnosis | Magnetic Resonance Imaging | Leukemia, Myeloid, Acute - diagnosis | Comparative Genomic Hybridization | Craniofacial Abnormalities - diagnosis | Antineoplastic Combined Chemotherapy Protocols - therapeutic use | Abnormalities, Multiple - diagnosis | Intellectual Disability - diagnosis | Lissencephaly - genetics | Mutation | Lymphomas | Missense mutation | Winter | Myeloid leukemia | Leukemia | Chromosome 7 | Lymphatic leukemia | Acute myeloid leukemia | Lymphoma | Mental retardation | Cancer
Journal Article
ENT Journal, ISSN 0145-5613, 9/2016, Volume 95, Issue 9, pp. E28 - E29
Journal Article