-O Bartsch Researcher Activity Profile

Research Author Detailed Information 

O Bartsch Publication Rate By Year

O Bartsch has published 2 paper(s) in 1993, 5 paper(s) in 2007, 1 paper(s) in 2008, for a total of 8 research publications in total.

O O Bartsch Author Information

LAST NAME: bartsch

FIRST NAME: O

INITIALS: o

AFFILIATION:

Papers

O Bartsch's Publication Record

1. Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis. Year Published: 2007
Institute for Human Genetics, Johannes Gutenberg University, Mainz (Germany).
2. Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis. Year Published: 2007
Institute for Human Genetics, Johannes Gutenberg University, Mainz, Germany. bartsch@humgen.klinik.uni-mainz.de
3. Two Novel Deletions (Array CGH Findings) in Pigment Dispersion Syndrome. Year Published: 2007
Department of Human Biology and Genetics, Institute of General and Molecular Pathology, University of Tartu, Tartu, Estonia.
4. Acrocallosal syndrome: association with cystic malformation of the brain and neurodevelopmental aspects. Year Published: 1993
5. Two novel deletions (array CGH findings) in pigment dispersion syndrome. Year Published: 2007
Department of Human Biology and Genetics, Institute of General and Molecular Pathology, University of Tartu, Tartu, Estonia. ruth.mikelsaar@ut.ee
6. Acrocallosal syndrome: association with cystic malformation of the brain and neurodevelopmental aspects. Year Published: 1993
7. Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis. Year Published: 2007
Institute for Human Genetics, Johannes Gutenberg University, Mainz, Germany. bartsch@humgen.klinik.uni-mainz.de
8. Girl with partial turner syndrome and absence epilepsy. Year Published: 2008
Department of Pediatrics, University of Tartu, Tartu, Estonia.