TY  - GEN
AU  - Netchine,Irène
AU  - Rossignol,Sylvie
AU  - Dufourg,Marie-Noëlle
AU  - Azzi,Salah
AU  - Rousseau,Alexandra
AU  - Perin,Laurence
AU  - Houang,Muriel
AU  - Steunou,Virginie
AU  - Esteva,Blandine
AU  - Thibaud,Nathalie
AU  - Demay,Marie-Charles Raux
AU  - Danton,Fabienne
AU  - Petriczko,Elzbieta
AU  - Bertrand,Anne-Marie
AU  - Heinrichs,Claudine
AU  - Carel,Jean-Claude
AU  - Loeuille,Guy-André
AU  - Pinto,Graziella
AU  - Jacquemont,Marie-Line
AU  - Gicquel,Christine
AU  - Cabrol,Sylvie
AU  - Le Bouc,Yves
TI  - 11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations
SN  - 0021-972X
PY  - 2007///0917
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Aging
KW  - metabolism
KW  - Chromosomes, Human, Pair 7
KW  - DNA
KW  - Face
KW  - abnormalities
KW  - Female
KW  - Fetal Growth Retardation
KW  - Genomic Imprinting
KW  - Humans
KW  - Infant, Newborn
KW  - Infant, Small for Gestational Age
KW  - physiology
KW  - Insulin-Like Growth Factor II
KW  - Male
KW  - Methylation
KW  - Mutation
KW  - Phenotype
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1210/jc.2007-0354
ER  -