Brunner, Han G. 1956-
Brunner, Han
Brunner, Han (Henri Gerrit), 1956-
Han Brunner
VIAF ID: 288931597 ( Personal )
Permalink: http://viaf.org/viaf/288931597
Preferred Forms
- 100 1 _ ‡a Brunner, Han
- 100 1 _ ‡a Brunner, Han G. ‡d 1956-
-
- 100 0 _ ‡a Han Brunner
4xx's: Alternate Name Forms (9)
5xx's: Related Names (2)
Works
Title | Sources |
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Ciliary dyneins and dynein related ciliopathies | |
Clinical and molecular delineation of the 17q21.31 microdeletion syndrome | |
Genetic studies in myotonic dystrophy | |
Genetisch onderzoek en advisering | |
Human Intellectual Disability Genes Form Conserved Functional Modules in Drosophila | |
Klinische genetica in de praktijk | |
Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-Acromelic (Waardenburg Anophthalmia) syndrome in humans and mice | |
Mendel of biometrie? | |
Spectrum of genetic variants in a cohort of 37 laterality defect cases | |
Ubiquitin Ligases of the N-End Rule Pathway: Assessment of Mutations in UBR1 That Cause the Johanson-Blizzard Syndrome |