Literature DB >> 874654

Familial splenic anomaly syndrome.

S C Chen, P L Monteleone.   

Abstract

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Year:  1977        PMID： 874654     DOI： 10.1016/s0022-3476(77)80476-9

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


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  2 in total

1.  Mutations in ZIC3 and ACVR2B are a common cause of heterotaxy and associated cardiovascular anomalies.

Authors:  Lijiang Ma; Elif Seda Selamet Tierney; Teresa Lee; Patricia Lanzano; Wendy K Chung
Journal:  Cardiol Young       Date:  2011-08-25       Impact factor: 1.093

2.  Asplenia and polysplenia syndromes with abnormalities of lateralisation in a sibship.

Authors:  J Zlotogora; E Elian
Journal:  J Med Genet       Date:  1981-08       Impact factor: 6.318
  2 in total

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