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You searched for: Author/Creator Hofmann, Andrea

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1. Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVs. Issue 1 (December 2016)

2. Array‐based molecular karyotyping in fetal brain malformations: Identification of novel candidate genes and chromosomal regions. Issue 1 (17th December 2015)

3. CNV analysis in 169 patients with bladder exstrophy-epispadias complex. Issue 1 (December 2016)

8. Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palate. Issue 9 (7th July 2016)

9. Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study. Issue 10023 (12th March 2016)

10. Genome-wide transcriptome induced by nickel in human monocytes. (1st October 2016)