ICR1 epimutations in 11p15 are restricted to patients with Silver-Russell syndrome features

Journal of Pediatric Endocrinology and Metabolism

Volumn 21, Issue 1, 2008, Pages 59-62

  Eggermann, Thomas ^a   Meyer, Esther ^a,b   Caglayan, A Okay ^c   Dundar, Munis ^c   Schonherr N ^a  

^a RWTH AACHEN UNIVERSITY   (Germany)

^b UNIVERSITY DEPARTMENT OF MEDICINE   (United Kingdom)

^c ERCIYES UNIVERSITY   (Turkey)

Author keywords

11p15 epimutation; Growth retardation; Maternal uniparental disomy 7; Silver Russell syndrome

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 11P; CHROMOSOME 7; CHROMOSOME MUTATION; CLINICAL FEATURE; CONTROLLED STUDY; GENETIC HETEROGENEITY; GENETIC SCREENING; GROWTH RETARDATION; HUMAN; INTRAUTERINE GROWTH RETARDATION; MAJOR CLINICAL STUDY; MUTATIONAL ANALYSIS; SILVER RUSSELL SYNDROME; TELOMERE; UNIPARENTAL DISOMY; CHROMOSOME 11; DNA METHYLATION; FACE ASYMMETRY; GENETICS; GENOME IMPRINTING; GROWTH DISORDER; MUTATION; SYNDROME;

DNA;

CHROMOSOMES, HUMAN, PAIR 11; DNA; DNA METHYLATION; FACIAL ASYMMETRY; FETAL GROWTH RETARDATION; GENETIC SCREENING; GENOMIC IMPRINTING; GROWTH DISORDERS; HUMANS; MUTATION; SYNDROME; UNIPARENTAL DISOMY;

EID: 40449100468     PISSN: 0334018X     EISSN: None     Source Type: Journal    
DOI: 10.1515/JPEM.2008.21.1.59     Document Type: Article

References (10)