Back to Search

FORBES PORTER, M.D.

M.D.

NPI: 1285920579Individual

Specialties, Licenses & Credentials

Clinical Genetics (M.D.) PhysicianPrimary

Medical Genetics — Clinical Genetics (M.D.)

Code: 207SG0201X

D0045118(MD)
Pediatrics Physician

Pediatrics

Code: 208000000X

D0045118(MD)

Research & Publications (20)

Smith-Lemli-Opitz syndrome: pathogenesis, diagnosis and management.
PMID 18285838·Eur J Hum Genet·2008
6-review
Cholesterol precursors and facial clefting.
PMID 16955133·J Clin Invest·2006
7-preclinical
Human malformation syndromes due to inborn errors of cholesterol synthesis.
PMID 14631207·Curr Opin Pediatr·2003
6-review
Malformation syndromes due to inborn errors of cholesterol synthesis.
PMID 12235098·J Clin Invest·2002
6-review
Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type C.
PMID 19415691·Am J Med Genet B Neuropsychiatr Genet·2010
8-other
Search for second-class currents in tau;{-} --> omegapi;{-}nu_{tau}.
PMID 19659341·Phys Rev Lett·2009
8-other
Evidence for X(3872)-->psi(2S)gamma in B(+/-)-->X(3872)K(+/-) decays and a study of B-->cc[over ]gammaK.
PMID 19392347·Phys Rev Lett·2009
8-other
Direct CP, lepton flavor, and isospin asymmetries in the decays B-->K(*)l+l-.
PMID 19392508·Phys Rev Lett·2009
8-other
Improved measurement of B+ --> rho+ rho0 and determination of the quark-mixing phase angle alpha.
PMID 19392426·Phys Rev Lett·2009
8-other
Measurement of B-->Xgamma decays and determination of |Vtd/Vts|.
PMID 19518698·Phys Rev Lett·2009
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
10 CENTER DR, 10-CRC, ROOM 5-2571
BETHESDA, MD 20892

Quick Facts

NPI
1285920579
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
2
Locations
1
Publications
20

Are you this provider?

Claim Your Profile