Weaver syndrome andEZH2mutations: Clarifying the clinical phenotype

Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height

(2015) Katrina Tatton-Brown et al.   Oncotarget

Mutations in EZH2 Cause Weaver Syndrome

(2011) William T. Gibson et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Aberrations of EZH2 in Cancer

(2011) A. Chase et al.   CLINICAL CANCER RESEARCH

Mutations in CEP57 cause mosaic variegated aneuploidy syndrome

(2011) Katie Snape et al.   NATURE GENETICS

Acute lymphoblastic leukemia in Weaver syndrome

(2010) Lina Basel-Vanagaite   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Twins and their mildly affected mother with Weaver syndrome

(2010) M. Dumić et al.   CLINICAL GENETICS

A Weaver-like syndrome in a Japanese boy

(2010) Masato Tsukahara et al.   CLINICAL GENETICS

Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin

(2010) Ryan D Morin et al.   NATURE GENETICS

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders

(2010) Thomas Ernst et al.   NATURE GENETICS

Coordinated activities of wild-type plus mutant EZH2 drive tumor-associated hypertrimethylation of lysine 27 on histone H3 (H3K27) in human B-cell lymphomas

(2010) C. J. Sneeringer et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Treatment of macroglossia in a child with Weaver syndrome

(2008) I.A. Iatrou et al.   INTERNATIONAL JOURNAL OF ORAL AND MAXILLOFACIAL SURGERY

Weaver Syndrome and Neuroblastoma

(2008) Don Coulter et al.   JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY