Parent-child exome sequencing identifies a de novo truncating mutation in TCF4 in non-syndromic intellectual disability (Q43551361)
Jump to navigation
Jump to search
scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Parent-child exome sequencing identifies a de novo truncating mutation in TCF4 in non-syndromic intellectual disability |
scientific article |
Statements
1 reference
Parent-child exome sequencing identifies a de novo truncating mutation in TCF4 in non-syndromic intellectual disability (English)
1 reference
G A Rouleau
1 reference
F F Hamdan
1 reference
H Daoud
1 reference
L Patry
1 reference
A Dionne-Laporte
1 reference
D Spiegelman
1 reference
S Dobrzeniecka
1 reference
J L Michaud
1 reference
4 June 2012
1 reference
1 reference
83
1 reference
2
1 reference
198-200
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference