Literature DB >> 24055528

Description of another case of 3q26.33-3q27.2 microdeletion supports a recognizable phenotype.

Yuri A Zarate1, Carla Bell, Brad Schaefer.   

Abstract

Mesh：

Year:  2013        PMID： 24055528     DOI： 10.1016/j.ejmg.2013.09.004

Source DB:  PubMed          Journal:  Eur J Med Genet        ISSN： 1769-7212            Impact factor:   2.708


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  2 in total

1.  3q27.1 microdeletion causes prenatal and postnatal growth restriction and neurodevelopmental abnormalities.

Authors:  Subit Barua; Elaine M Pereira; Vaidehi Jobanputra; Kwame Anyane-Yeboa; Brynn Levy; Jun Liao
Journal:  Mol Cytogenet       Date:  2022-03-03       Impact factor: 2.009

2.  An 8.4-Mb 3q26.33-3q28 microdeletion in a patient with blepharophimosis-intellectual disability syndrome and a review of the literature.

Authors:  Katrin Õunap; Sander Pajusalu; Olga Zilina; Tiia Reimand; Riina Žordania
Journal:  Clin Case Rep       Date:  2016-07-22
  2 in total

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