Erratum: A novel mutation in EED associated with overgrowth (Journal of Human Genetics (2015) 60 (339-342) DOI: 10.1038/jhg.2015.26);A novel mutation in EED associated with overgrowth

Journal of Human Genetics

Volumn 60, Issue 6, 2015, Pages 339-342

  Cohen, Ana S A ^a,b   Tuysuz, Beyhan ^c   Shen, Yaoqing ^d   Bhalla, Sanjiv K ^e   Jones, Steven J M ^a,d,f   Gibson, William T ^a,b  

^a UNIVERSITY OF BRITISH COLUMBIA   (Canada)

^b BC CHILDREN S HOSPITAL   (Canada)

^c ISTANBUL UNIVERSITY   (Turkey)

^d BRITISH COLUMBIA CANCER AGENCY   (Canada)

^e SURREY MEMORIAL HOSPITAL   (Canada)

^f SIMON FRASER UNIVERSITY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

PHENYTOIN; PRIMIDONE; EED PROTEIN, HUMAN; POLYCOMB REPRESSIVE COMPLEX 2;

ADOLESCENT; AMINO ACID SUBSTITUTION; ARTICLE; BONE AGE; CASE REPORT; CATARACT EXTRACTION; CHILD; CONTROLLED STUDY; CRYPTORCHISM; EED GENE; EPILEPSY; EXOME; GENE; GENE SILENCING; GENETIC ASSOCIATION; GENOTYPE PHENOTYPE CORRELATION; GROWTH DISORDER; HUMAN; HYPERTELORISM; INTELLECTUAL IMPAIRMENT; ISCHEMIA; KYPHOSCOLIOSIS; LARGE EAR; LEG AMPUTATION; MACROCEPHALY; MALE; MISSENSE MUTATION; MITRAL VALVE REGURGITATION; MOTOR PERFORMANCE; MUTATIONAL ANALYSIS; MYOPIA; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; PATELLA DISLOCATION; PATHOGENESIS; PEDIGREE; PHENOTYPE; PIGMENTED NEVUS; PRESCHOOL CHILD; RETROGNATHIA; SCHOOL CHILD; SCOLIOSIS; SEIZURE; SKELETON MALFORMATION; SPEECH DELAY; TALL STATURE; UMBILICAL HERNIA; WEAVER SYNDROME; ABNORMALITIES, MULTIPLE; ADULT; CONGENITAL HYPOTHYROIDISM; CRANIOFACIAL ABNORMALITIES; DIFFERENTIAL DIAGNOSIS; GENETICS; GROWTH DISORDERS; HAND DEFORMITIES, CONGENITAL; NUCLEOTIDE SEQUENCE;

ABNORMALITIES, MULTIPLE; ADULT; CONGENITAL HYPOTHYROIDISM; CRANIOFACIAL ABNORMALITIES; DIAGNOSIS, DIFFERENTIAL; DNA MUTATIONAL ANALYSIS; GROWTH DISORDERS; HAND DEFORMITIES, CONGENITAL; HUMANS; MALE; MUTATION, MISSENSE; POLYCOMB REPRESSIVE COMPLEX 2;

EID: 84932600625     PISSN: 14345161     EISSN: 1435232X     Source Type: Journal    
DOI: 10.1038/jhg.2016.156     Document Type: Erratum

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