Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis (Q34386278)
Jump to navigation
Jump to search
scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis |
scientific article |
Statements
Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis (English)
Buiting K
Dittrich B
Gross S
Lich C
Färber C
Buchholz T
Smith E
Bürger J
Barth-Witte U
Janssen B
Abeliovich D
Lerer I
van den Ouweland AM
Halley DJ
Schrander-Stumpel C
Smeets H
Meinecke P
Malcolm S
Gardner A
Lalande M
Nicholls RD
Friend K
Schulze A
Matthijs G
Kokkonen H
Hilbert P
Van Maldergem L
Glover G
Carbonell P
Willems P
Gillessen-Kaesbach G
Horsthemke B
1 July 1998
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference