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You searched for: Author/Creator Braun, Daniela A.

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1. Cystic kidneys in fetal Walker–Warburg syndrome with POMT2 mutation: Intrafamilial phenotypic variability in four siblings and review of literature. Issue 10 (17th August 2017)

2. Mutations in WDR4 as a new cause of Galloway–Mowat syndrome. Issue 11 (6th August 2018)

3. Targeted Resequencing of 29 Candidate Genes and Mouse Expression Studies Implicate ZIC3 and FOXF1 in Human VATER/VACTERL Association. Issue 12 (14th September 2015)

4. Whole Exome Sequencing Reveals a Monogenic Cause of Disease in ≈43% of 35 Families With Midaortic Syndrome. Issue 4 (April 2018)