Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders (Q45340913)
Jump to navigation
Jump to search
scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders |
scientific article |
Statements
1 reference
Analysis of the IGF2/H19 imprinting control region uncovers new genetic defects, including mutations of OCT-binding sequences, in patients with 11p15 fetal growth disorders (English)
1 reference
1 reference
Julie Demars
1 reference
Mansur Ennuri Shmela
1 reference
Sylvie Rossignol
1 reference
Jun Okabe
1 reference
Irène Netchine
1 reference
Sylvie Cabrol
1 reference
Albert David
1 reference
Yves Le Bouc
1 reference
Christine Gicquel
1 reference
9 December 2009
1 reference
1 reference
Identifiers
1 reference