Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome (Q33592563)
Jump to navigation
Jump to search
scientific article published on March 1, 1988
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome |
scientific article published on March 1, 1988 |
Statements
1 reference
Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome (English)
1 reference
1 reference
H. Santos
J. Mateus
1 March 1988
1 reference
1 reference
204-205
1 reference
Identifiers
1 reference
1 reference