DR. ERIC DOUGLAS GREEN, M.D.
Medical Practice in Bethesda, MD
License number
Maryland 100218
Category
Medical Practice
Type
Clinical Pathology
Address
Address
31 Center Dr Building 31 ROOM 4B09, Bethesda, MD 20892
Phone
(301) 496-0844
(301) 402-0837 (Fax)
(301) 402-0837 (Fax)
Personal information
See more information about ERIC DOUGLAS GREEN at radaris.comName
Address
Phone
4406 23Rd Pkwy, Temple Hills, MD 20748
5702 Radecke Ave APT C2, Baltimore, MD 21206
5571 Elderon Ave, Baltimore, MD 21215
50 Hearthstone Ct APT C, Annapolis, MD 21403
Professional information
See more information about ERIC DOUGLAS GREEN at trustoria.com
Eric Douglas Green, Bethesda MD
Eric Douglas Green, Bethesda MD
Specialties:
Pathology
Work:
Eric D Levine
31 Ctr Dr #Building, Bethesda, MD 20892
31 Ctr Dr #Building, Bethesda, MD 20892
Dr. Eric D Green, Bethesda MD - MD (Doctor of Medicine)
Dr. Eric D Green, Bethesda MD - MD (Doctor of Medicine)
Specialties:
Anatomic & Clinical Pathology, Clinical Genetics
Address:
31 Ctr Dr SUITE 31, Bethesda 20892
(301) 496-0844 (Phone), (301) 402-0837 (Fax)
(301) 496-0844 (Phone), (301) 402-0837 (Fax)
Languages:
English
Education:
Medical School
Washington Center / School of Medicine
Graduated: 1987
Washington Center / School of Medicine
Graduated: 1987
Eric Douglas Green, Bethesda MD
Eric Douglas Green, Bethesda MD
Specialties:
Pathologist
Address:
31 Center Dr, Bethesda, MD 20892
Methods For Identifying Mutations In Coding And Non-Coding Dna
Methods For Identifying Mutations In Coding And Non-Coding Dna
US Patent:
2010004, Feb 25, 2010
Filed:
May 26, 2006
Appl. No.:
11/920908
Inventors:
Aravinda Chakravarti - Lutherville MD, US
Eileen Sproat Emison - Elkridge MD, US
Andrew Smythe McCallion - Baltimore MD, US
Eric Green - Bethesda MD, US
Eileen Sproat Emison - Elkridge MD, US
Andrew Smythe McCallion - Baltimore MD, US
Eric Green - Bethesda MD, US
Assignee:
The Johns Hopkins University - Baltimore MD
International Classification:
C12Q 1/68
US Classification:
435 6
Abstract:
The present invention provides methods of identifying mutations in nucleic acid. Also provided herein are methods of identifying subjects having Hirschsprung disease risk and diagnostic markers for Hirschsprung disease.