Literature DB >> 19764038

Interstitial deletion 2p11.2-p12: further delineation.

Karin Writzl1, Luca Lovrecić, Borut Peterlin.   

Abstract

Mesh：

Year:  2009        PMID： 19764038     DOI： 10.1002/ajmg.a.33064

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  2 in total

1.  A recurrent deletion syndrome at chromosome bands 2p11.2-2p12 flanked by segmental duplications at the breakpoints and including REEP1.

Authors:  Servi J C Stevens; Eveline W Blom; Ingrid T J Siegelaer; Eric E J G L Smeets
Journal:  Eur J Hum Genet       Date:  2014-07-02       Impact factor: 4.246

2.  An intragenic deletion within CTNNA2 intron 7 in a boy with short stature and speech delay: A case report.

Authors:  Valeria Paganelli; Mara Giordano; Cristina Meazza; Lucia Schena; Mauro Bozzola
Journal:  SAGE Open Med Case Rep       Date:  2017-02-15
  2 in total

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