Literature DB >> 19508422

Congenital diaphragmatic abnormalities in arterial tortuosity syndrome patients who carry mutations in the SLC2A10 gene.

S H E Zaidi, S Meyer, I Peltekova, A S Teebi, M Faiyaz-Ul-Haque.   

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Year:  2009        PMID： 19508422     DOI： 10.1111/j.1399-0004.2009.01165.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  3 in total

Review 1.  Underlying genetic etiologies of congenital diaphragmatic hernia.

Authors:  Daryl A Scott; Yoel Gofin; Aliska M Berry; April D Adams
Journal:  Prenat Diagn       Date:  2022-01-22       Impact factor: 3.050

2.  Clinical Variability in Two Macedonian Families with Arterial Tortuosity Syndrome.

Authors:  M Kocova; R Kacarska; K Kuzevska-Maneva; S Prijic; M Lazareska; C Dordoni; M Ritelli; M Colombi
Journal:  Balkan J Med Genet       Date:  2018-10-29       Impact factor: 0.519

Review 3.  Unraveling the Genetics of Congenital Diaphragmatic Hernia: An Ongoing Challenge.

Authors:  Erwin Brosens; Nina C J Peters; Kim S van Weelden; Charlotte Bendixen; Rutger W W Brouwer; Frank Sleutels; Hennie T Bruggenwirth; Wilfred F J van Ijcken; Danielle C M Veenma; Suzan C M Cochius-Den Otter; Rene M H Wijnen; Alex J Eggink; Marieke F van Dooren; Heiko Martin Reutter; Robbert J Rottier; J Marco Schnater; Dick Tibboel; Annelies de Klein
Journal:  Front Pediatr       Date:  2022-02-03       Impact factor: 3.418
  3 in total

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