November 29, 2023
4:10PM
-
5:05PM
Room 155 Jennings Hall
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2023-11-29 16:10:00
2023-11-29 17:05:00
Molecular Genetics Seminar: Dr. Rolf Stottmann
Join us for Dr. Rolf Stottmann's seminar at 4:10 in room 155 Jennings.
"Genetics of Congenital Anomalies of the Brain and Face”
Dr. Stottmann joined the Institute for Genomic Medicine at Nationwide Children’s Hospital as a principal investigator in 2021 and is an associate professor at The Ohio State University College of Medicine. He has an enduring interest in the genetics of structural birth defects with a focus on structural brain malformations and disrupted craniofacial skeletal development. Dr. Stottmann's lab uses a combination of human and mouse genetics to identify and study rare genetic variants which cause these congenital malformations.
Host: Susan Cole, cole.354@osu.edu
Room 155 Jennings Hall
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America/New_York
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Date Range
2023-11-29 16:10:00
2023-11-29 17:05:00
Molecular Genetics Seminar: Dr. Rolf Stottmann
Join us for Dr. Rolf Stottmann's seminar at 4:10 in room 155 Jennings.
"Genetics of Congenital Anomalies of the Brain and Face”
Dr. Stottmann joined the Institute for Genomic Medicine at Nationwide Children’s Hospital as a principal investigator in 2021 and is an associate professor at The Ohio State University College of Medicine. He has an enduring interest in the genetics of structural birth defects with a focus on structural brain malformations and disrupted craniofacial skeletal development. Dr. Stottmann's lab uses a combination of human and mouse genetics to identify and study rare genetic variants which cause these congenital malformations.
Host: Susan Cole, cole.354@osu.edu
Room 155 Jennings Hall
America/New_York
public
Join us for Dr. Rolf Stottmann's seminar at 4:10 in room 155 Jennings.
"Genetics of Congenital Anomalies of the Brain and Face”
Dr. Stottmann joined the Institute for Genomic Medicine at Nationwide Children’s Hospital as a principal investigator in 2021 and is an associate professor at The Ohio State University College of Medicine. He has an enduring interest in the genetics of structural birth defects with a focus on structural brain malformations and disrupted craniofacial skeletal development. Dr. Stottmann's lab uses a combination of human and mouse genetics to identify and study rare genetic variants which cause these congenital malformations.
Host: Susan Cole, cole.354@osu.edu
