Literature DB >> 18512227

Kidney abnormalities in persons with monosomy 15q26.

Iosif W Lurie1.   

Abstract

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Year:  2008        PMID： 18512227     DOI： 10.1002/ajmg.a.32333

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


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  3 in total

1.  Array Characterization of Prenatally Diagnosed 15q26 Microdeletion and 2q37.1 Duplication: Report of a New Case with Multicystic Kidneys and Review of the Literature.

Authors:  Molka Kammoun; Wafa Slimani; Hanene Hannachi; Mohamed Bibi; Ali Saad; Soumaya Mougou-Zerelli
Journal:  J Pediatr Genet       Date:  2017-04-26

Review 2.  Choose your destiny: Make a cell fate decision with COUP-TFII.

Authors:  San-Pin Wu; Cheng-Tai Yu; Sophia Y Tsai; Ming-Jer Tsai
Journal:  J Steroid Biochem Mol Biol       Date:  2015-12-02       Impact factor: 4.292

3.  15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review.

Authors:  Yahya Benbouchta; Nicole De Leeuw; Saadia Amasdl; Aziza Sbiti; Dominique Smeets; Khalid Sadki; Abdelaziz Sefiani
Journal:  Ital J Pediatr       Date:  2021-09-16       Impact factor: 2.638
  3 in total

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