A novel autosomal recessive malformation syndrome associated with developmental delay and distinctive facies maps to 16ptel in the Hutterite population. (Q51907635)
Jump to navigation
Jump to search
scientific article published in June 2010
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A novel autosomal recessive malformation syndrome associated with developmental delay and distinctive facies maps to 16ptel in the Hutterite population. |
scientific article published in June 2010 |
Statements
A novel autosomal recessive malformation syndrome associated with developmental delay and distinctive facies maps to 16ptel in the Hutterite population. (English)
1 reference
Kym M Boycott
1 reference
Chandree Beaulieu
1 reference
A Micheil Innes
1 reference
Jillian S Parboosingh
1 reference
Erik G Puffenberger
1 reference
D Ross McLeod
1 reference
1 June 2010
1 reference
152A
1 reference
6
1 reference
1349-1356
1 reference
Identifiers
1 reference