Literature DB >> 9851750

Germline RET codon 918 mutation in apparently isolated intestinal ganglioneuromatosis.

C Eng1, D J Marsh, B G Robinson, C W Chow, M A Patton, M C Southey, D J Venter, B A Ponder, P J Milla, V V Smith.   

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Year:  1998        PMID： 9851750     DOI： 10.1210/jcem.83.12.5352

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN： 0021-972X            Impact factor:   5.958


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  3 in total

Review 1.  Advances in understanding functional variations in the Hirschsprung disease spectrum (variant Hirschsprung disease).

Authors:  S W Moore
Journal:  Pediatr Surg Int       Date:  2016-12-17       Impact factor: 1.827

Review 2.  [Motility disorders of the esophagus].

Authors:  E Bruder; A-L Rougemont; R I Furlano; J F Schneider; J Mayr; F-M Haecker; K Beier; J Schneider; P Weber; T Berberich; G Cathomas; W A Meier-Ruge
Journal:  Pathologe       Date:  2013-03       Impact factor: 1.011

3.  Diffuse intestinal ganglioneuromatosis in a child.

Authors:  Mika A B Matthews; Brent H Adler; Michael A Arnold; Soma Kumar; Ryan Carvalho; Gail E Besner
Journal:  J Pediatr Surg       Date:  2013-05       Impact factor: 2.545
  3 in total

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