Infantile hyperinsulinism associated with enteropathy, deafness and renal tubulopathy: clinical manifestations of a syndrome caused by a contiguous gene deletion located on chromosome 11p. (Q45220880)
Jump to navigation
Jump to search
scientific article published in December 2004
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Infantile hyperinsulinism associated with enteropathy, deafness and renal tubulopathy: clinical manifestations of a syndrome caused by a contiguous gene deletion located on chromosome 11p. |
scientific article published in December 2004 |
Statements
1 reference
Infantile hyperinsulinism associated with enteropathy, deafness and renal tubulopathy: clinical manifestations of a syndrome caused by a contiguous gene deletion located on chromosome 11p. (English)
1 reference
1 reference
Khalid Hussain
1 reference
Maria Bitner-Glindzicz
1 reference
Diana Blaydon
1 reference
Keith J Lindley
1 reference
Dorothy A Thompson
1 reference
Tony Kriss
1 reference
Kaukat Rajput
1 reference
Dina G Ramadan
1 reference
Z Al-Mazidi
1 reference
Mark J Dunne
1 reference
Albert Aynsley-Green
1 reference
1 December 2004
1 reference
1 reference
17
1 reference
12
1 reference
1613-1621
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference