Dr. Garry R Cutting M.D.
Pediatrician
1800 Orleans Street Sheikh Zayed Tower S Baltimore MD, 21287About
Dr. Garry Cutting is a pediatrician practicing in Baltimore, MD. Dr. Cutting is a doctor who specializes in the health care of children. As a pedicatrician, Dr. Cutting diagnoses and treats infections, injuries, diseases and other disorders in children. Pediatricians typically work with infants, children, teenagers and young adults up to age 21. They practice medical care as well as preventative health care. Dr. Cutting can oversee and manage the physical, mental and emotional health of their patients.
Education and Training
Univ Of Ct Sch Of Med- Farmington Ct 1983
Univ Of Ct Sch Of Med 1983
University of Connecticut School of Medicine 1983
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
PediatricsAmerican Board of PediatricsABP
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Clinical and genetic studies of an autosomal dominant cone-rod dystrophy with features of Stargardt disease.
- Identification of 70 amino acids important for GABA(C) receptor rho1 subunit assembly.
- Expression of the voltage-gated chloride channel ClC-2 in rod bipolar cells of the rat retina.
- A PDZ-interacting domain in CFTR is an apical membrane polarization signal.
- Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia.
- Effects of cystic fibrosis and congenital bilateral absence of the vas deferens-associated mutations on cystic fibrosis transmembrane conductance regulator-mediated regulation of separate channels.
- Mutation analysis of GABRR1 and GABRR2 in autosomal recessive retinitis pigmentosa.
- The PDZ-interacting domain of cystic fibrosis transmembrane conductance regulator is required for functional expression in the apical plasma membrane.
- Genotype-phenotype relationships in cystic fibrosis.
- Simplified multiplex-PCR diagnosis of common southeast asian deletional determinants of alpha-thalassemia.
- Mutation in the gene responsible for cystic fibrosis and predisposition to chronic rhinosinusitis in the general population.
- A PDZ-binding motif is essential but not sufficient to localize the C terminus of CFTR to the apical membrane.
- Developmentally regulated expression of GABA receptor rho1 and rho2 subunits, L7 and cone-rod homeobox (CRX) genes in mouse retina.
- A Golgi-associated PDZ domain protein modulates cystic fibrosis transmembrane regulator plasma membrane expression.
- ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: role in diagnosis and clinical correlations.
Treatments
- Birth Defects
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