Literature DB >> 4022703

Meningomyelocele and Hirschprung disease: theoretical and clinical significance.

R G Merkler, S B Solish, A L Scherzer.   

Abstract

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Year:  1985        PMID： 4022703

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  4 in total

Review 1.  Hirschsprung disease, associated syndromes, and genetics: a review.

Authors:  J Amiel; S Lyonnet
Journal:  J Med Genet       Date:  2001-11       Impact factor: 6.318

Review 2.  Hirschsprung's disease--a review.

Authors:  C M Doig
Journal:  Int J Colorectal Dis       Date:  1991-02       Impact factor: 2.571

3.  Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness: a new autosomal recessive syndrome.

Authors:  H Santos; J Mateus; M J Leal
Journal:  J Med Genet       Date:  1988-03       Impact factor: 6.318

Review 4.  The contribution of associated congenital anomalies in understanding Hirschsprung's disease.

Authors:  S W Moore
Journal:  Pediatr Surg Int       Date:  2006-03-04       Impact factor: 1.827
  4 in total

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