Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus.

Author:

Edery P,Pelet A,Mulligan L M,Abel L,Attie T,Dow E,Bonneau D,David A,Flintoff W,Jan D

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference27 articles.

1. Hirschsprung's disease in the newborn;Polley, T.Z.; Coran, A.G.;Pediatr Surg Int,1986

2. The neurocristopathies; a unifying concept of disease arising in neural crest maldevelopment;Bolande, R.P.;Hum Pathol,1973

3. Hirschsprung disease: mapping of a dominant gene closely linked to the RET locus on the proximal long arm of chromosome 10;Edery, P.; Lyonnet, S.; Abel, L.;Am J Hum Genet (Suppl),1993

4. Close linkage with the RET proto-oncogene and boundaries of deletion mutations in autosomal dominant Hirschsprung disease;Luo, Y.; Ceccherini, I.; Pasini, B.;Hum Molec Genet,1993

5. Point mutations affecting the tyrosine kinase domain of the RET protooncogene in Hirschsprung's disease;Romeo, G.; Ronchetto, P.; Luo, Y.;Nature,1994

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