Literature DB >> 14339396

FAMILIAL ABSENCE OF MYENTERIC PLEXUS (CONGENITAL MEGACOLON).

B EMANUEL, M P PADORR, O SWENSON.   

Abstract

Entities:  

Keywords:  CHROMOSOMES; COLOSTOMY; DISEASES IN TWINS; GENETICS, HUMAN; INFANT; INFANT, NEWBORN; INFANT, NEWBORN, DISEASES; MEGACOLON

Mesh：

Year:  1965        PMID： 14339396     DOI： 10.1016/s0022-3476(65)80398-5

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


× No keyword cloud information.
  6 in total

1.  Genetic considerations in aganglionic megacolon and imperforation.

Authors:  W G Smith
Journal:  Proc R Soc Med       Date:  1970

Review 2.  Hirschsprung's disease.

Authors:  T Ehrenpreis
Journal:  Am J Dig Dis       Date:  1971-11

3.  Hirschsprung's disease associated with congenital heart malformation, broad big toes, and ulnar polydactyly in sibs: a case for fetoscopy.

Authors:  K M Laurence; R Prosser; I Rocker; J F Pearson; C Richard
Journal:  J Med Genet       Date:  1975-12       Impact factor: 6.318

Review 4.  Hirschsprung's disease in twins: a systematic review and meta-analysis.

Authors:  D Henderson; J Zimmer; H Nakamura; Prem Puri
Journal:  Pediatr Surg Int       Date:  2017-06-10       Impact factor: 1.827

5.  Children of those treated surgically for Hirschsprung's disease.

Authors:  C O Carter; K Evans; V Hickman
Journal:  J Med Genet       Date:  1981-04       Impact factor: 6.318

Review 6.  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
  6 in total

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