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JEAN-JOSEPH DESIR, M.D
M.D
Student in an Organized Health Care Education/Training Program
NPI: 1346402252Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training ProgramPrimary
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Research & Publications (5)
Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome).
PMID 18922146·Orphanet J Rare Dis·2008
6-review
Primary microcephaly with ASPM mutation shows simplified cortical gyration with antero-posterior gradient pre- and post-natally.
PMID 18452193·Am J Med Genet A·2008
5-case
Borate transporter SLC4A11 mutations cause both Harboyan syndrome and non-syndromic corneal endothelial dystrophy.
PMID 17220209·J Med Genet·2007
8-other
Novel mutations in prenatal diagnosis of primary microcephaly.
PMID 17029297·Prenat Diagn·2006
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 800 POLY PL
BROOKLYN, NY 11209 - Phone
- (718) 836-6600
Quick Facts
- NPI
- 1346402252
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 5
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