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DR. JUDSON R BELMONT MD

MD

Otolaryngology Physician

NPI: 1285623595Individual

Specialties, Licenses & Credentials

Otolaryngology PhysicianPrimary

Otolaryngology

Code: 207Y00000X

7535(NH)

Research & Publications (20)

Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America.
PMID 18683858·Hum Mutat·2009
8-other
The futility of genomic counseling: essential role of electronic health records.
PMID 19439060·Genome Med·2009
8-other
Linkage analysis of left ventricular outflow tract malformations (aortic valve stenosis, coarctation of the aorta, and hypoplastic left heart syndrome).
PMID 19142209·Eur J Hum Genet·2009
8-other
BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects.
PMID 19367324·Eur J Hum Genet·2009
7-preclinical
20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits.
PMID 18812404·J Med Genet·2009
7-preclinical
Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations.
PMID 19064609·Hum Mol Genet·2009
8-other
An ancestry informative marker set for determining continental origin: validation and extension using human genome diversity panels.
PMID 19630973·BMC Genet·2009
8-other
Effectiveness of teaching cardiac auscultation to residents during an elective pediatric cardiology rotation.
PMID 18648718·Pediatr Cardiol·2008
8-other
Array-based DNA diagnostics: let the revolution begin.
PMID 17961075·Annu Rev Med·2008
6-review
Amerindian ancestry in Argentina is associated with increased risk for systemic lupus erythematosus.
PMID 18401351·Genes Immun·2008
8-other
Lipocalin 2 is required for BCR-ABL-induced tumorigenesis.
PMID 18663364·Oncogene·2008
7-preclinical
NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling.
PMID 18593716·Hum Mol Genet·2008
7-preclinical
Low-level mosaicism of trisomy 14: phenotypic and molecular characterization.
PMID 18412278·Am J Med Genet A·2008
5-case
Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly.
PMID 18538293·Am J Hum Genet·2008
7-preclinical
Human milk intake and retinopathy of prematurity in extremely low birth weight infants.
PMID 18762549·Pediatrics·2008
8-other
Characterization of the interactions of human ZIC3 mutants with GLI3.
PMID 17764085·Hum Mutat·2008
8-other
Analysis of East Asia genetic substructure using genome-wide SNP arrays.
PMID 19057645·PLoS One·2008
8-other
22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome.
PMID 18179902·Am J Hum Genet·2008
8-other
Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes.
PMID 18414210·Genet Med·2008
4-observational
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
PMID 19029900·Nat Genet·2008
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
130 TARRYTOWN RD
MANCHESTER, NH 03103
Practice locations map

Location

EAR NOSE THROAT PHYSICIANS & SURGEONS PA

130 TARRYTOWN RD, MANCHESTER, NH
(603) 669-0831

Quick Facts

NPI
1285623595
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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