TY  - GEN
AU  - Bartholdi,D
AU  - Krajewska-Walasek,M
AU  - Ounap,K
AU  - Gaspar,H
AU  - Chrzanowska,K H
AU  - Ilyana,H
AU  - Kayserili,H
AU  - Lurie,I W
AU  - Schinzel,A
AU  - Baumer,A
TI  - Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes
SN  - 1468-6244
PY  - 2009///0521
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Adolescent
KW  - Adult
KW  - Analysis of Variance
KW  - Child
KW  - Child, Preschool
KW  - Cohort Studies
KW  - Craniofacial Abnormalities
KW  - DNA Methylation
KW  - Epigenesis, Genetic
KW  - Female
KW  - Fetal Growth Retardation
KW  - Genomic Imprinting
KW  - Humans
KW  - Infant
KW  - Insulin-Like Growth Factor II
KW  - Male
KW  - Mutation
KW  - Phenotype
KW  - Pregnancy
KW  - Research Design
KW  - Syndrome
KW  - Uniparental Disomy
N1  - Publication Type: Letter; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1136/jmg.2008.061820
ER  -