Autosomal dominant transmission of congenital hypothyroidism, neonatal respiratory distress, and ataxia caused by a mutation of NKX2-1. (Q47947643)
Jump to navigation
Jump to search
scientific article published in August 2004
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Autosomal dominant transmission of congenital hypothyroidism, neonatal respiratory distress, and ataxia caused by a mutation of NKX2-1. |
scientific article published in August 2004 |
Statements
1 reference
Autosomal dominant transmission of congenital hypothyroidism, neonatal respiratory distress, and ataxia caused by a mutation of NKX2-1. (English)
1 reference
Daniel A Doyle
1 reference
Iris Gonzalez
1 reference
Becky Thomas
1 reference
Mena Scavina
1 reference
1 August 2004
1 reference
1 reference
145
1 reference
2
1 reference
190-193
1 reference
Identifiers
1 reference
1 reference