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Chin-To Fong
Concepts (205)
Concepts are derived automatically from a person's publications.
Cloud
Categories
Timeline
Details
In this concept cloud, the sizes of the concepts are based not only on the number of corresponding publications, but also how relevant the concepts are to the overall topics of the publications, how long ago the publications were written, whether the person was the first or senior author, and how many other people have written about the same topic. The largest concepts are those that are most unique to this person.
Abnormalities, Multiple
Acute Disease
Adolescent
Adrenal Gland Neoplasms
Adult
Age of Onset
Albinism, Oculocutaneous
Amikacin
Amino Acid Sequence
Ampicillin
Animals
Arginine Vasopressin
Attitude to Health
Autistic Disorder
Base Sequence
Blood
Blotting, Northern
Blotting, Southern
Body Height
Carcinoma
Cardiomyopathy, Dilated
Case-Control Studies
Cell Division
Cephalometry
Cerebral Cortex
Cerebral Ventricles
Child
Child Behavior
Child, Preschool
Choristoma
Chromosome Aberrations
Chromosome Banding
Chromosome Deletion
Chromosome Disorders
Chromosome Mapping
Chromosomes, Fungal
Chromosomes, Human, Pair 1
Chromosomes, Human, Pair 10
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 13
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 17
Chromosomes, Human, Pair 7
Cleft Lip
Cleft Palate
Clone Cells
Cloning, Molecular
Congenital Hypothyroidism
Connective Tissue Diseases
Consanguinity
Costa Rica
Cranial Nerve Neoplasms
Craniofacial Abnormalities
CREB-Binding Protein
Cross-Sectional Studies
Curriculum
Cystic Fibrosis
Developmental Disabilities
Diagnosis, Differential
Disease Progression
Disease Susceptibility
DNA
DNA Mutational Analysis
DNA Probes
DNA Restriction Enzymes
DNA, Neoplasm
Down Syndrome
Ear, External
Education, Medical
Energy Metabolism
Ethnic Groups
Face
Facial Asymmetry
Failure to Thrive
Family
Family Health
Fasciitis
Female
Fluorescent Antibody Technique
Foot Deformities, Congenital
Forecasting
Forkhead Transcription Factors
Frameshift Mutation
Gene Amplification
Gene Deletion
Gene Duplication
Gene Library
Gene Transfer Techniques
Genes, Dominant
Genes, myc
Genes, Neurofibromatosis 1
Genes, Tumor Suppressor
Genetic Diseases, Inborn
Genetic Heterogeneity
Genetic Linkage
Genetic Markers
Genetic Predisposition to Disease
Genetics
Genome, Human
Growth Disorders
Hand Deformities, Congenital
Health Behavior
Health Knowledge, Attitudes, Practice
Heart Diseases
Hermanski-Pudlak Syndrome
Heterozygote
Homozygote
Humans
Hypertension
Hyponatremia
Immunohistochemistry
In Situ Hybridization, Fluorescence
Infant
Infant, Newborn
Kanamycin
Karyotyping
Language Development Disorders
Leukemia
Liver Cirrhosis
Magnetic Resonance Imaging
Male
Maxilla
Maxillofacial Development
Membrane Proteins
Mental Disorders
Metabolism, Inborn Errors
Mice
Mice, Inbred C57BL
Mice, SCID
Microcephaly
Microscopy, Electron
Middle Aged
Molecular Sequence Data
Multiple Endocrine Neoplasia
Muscular Dystrophies
Mutation
Myasthenia Gravis
Nasal Bone
Nasal Septum
Neoplasm Staging
Neoplasm Transplantation
Neuroblastoma
Neurofibromin 2
Nucleic Acid Hybridization
Observer Variation
Oligonucleotide Array Sequence Analysis
Olivary Nucleus
Oncogenes
Osmolar Concentration
Ovarian Neoplasms
Parents
Pedigree
Phenotype
Pheochromocytoma
Plasmids
Ploidies
Polycystic Kidney, Autosomal Dominant
Polymerase Chain Reaction
Polymorphism, Restriction Fragment Length
Polymorphism, Single-Stranded Conformational
Prader-Willi Syndrome
Pregnancy
Prenatal Diagnosis
Prognosis
Prospective Studies
Proteins
Proto-Oncogene Proteins
Proto-Oncogene Proteins c-myc
Pseudogenes
Pseudomonas Infections
Puerto Rico
Quantitative Trait Loci
Repetitive Sequences, Nucleic Acid
Restriction Mapping
Retrospective Studies
Risk
Risk Factors
RNA Splicing
Rubinstein-Taybi Syndrome
S100 Proteins
Saline Solution, Hypertonic
Schizophrenia
Schwann Cells
Sepsis
Sequence Homology, Amino Acid
Sequence Homology, Nucleic Acid
Siblings
Sickle Cell Trait
Skull
Social Behavior
Speech Disorders
Statistics, Nonparametric
Syndrome
Thyroid Neoplasms
Ticarcillin
Time Factors
Trigeminal Nerve
Tumor Cells, Cultured
Velopharyngeal Insufficiency
Vimentin
Williams Syndrome
X Chromosome
Young Adult
Zellweger Syndrome
Visualizations
Concepts
Timeline
Cloud
Details
Co-Author Network
Timeline
Radial
Cluster
Details
Fong's Networks
Concepts
Derived automatically from this person's publications.
Congenital Hypothyroidism
Abnormalities, Multiple
Failure to Thrive
Chromosome Deletion
Chromosomes, Human, Pair 1
See all (205) concept(s)
_
Co-Authors
People in Profiles who have published with this person.
Tallents, Ross
Wang, Nancy
Lambert, David
Pearson, Thomas
DiGiovanni, Benedict
See all (22) people
_
Similar People
People who share similar concepts with this person.
Pichichero, Michael
Szilagyi, Peter
Moss, Arthur
Zareba, Wojciech
Halterman, Jill
See all (60) people
_
Same Department
People who are also in this person's primary department.
Caiola, Enrico
D'Aco, Kristin
Ho, Monique
Lagoe, Erin
Marcus, Carolina
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