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One or more keywords matched the following properties of Waggoner, Darrel J.
PropertyValue
overview I am a clinical geneticist and 50% of my effort is devoted to patient activity. I participate in a general genetics clinic one full day where with a team of genetic counselors and fellows we see a wide range of both adult and pediatric patients for evaluation, diagnosis, counseling and treatment for genetic disorders. In addition I am involved in several multidisciplinary clinics including Marfan and Craniofacial clinic. I am also involved in education throughout the university specifically in the medical school. I am interested in developing new and unique curriculum for integrating genetics into the four years of the medical school training and residency programs. I am the Program Director for the Genetics Laboratory Training Program in molecular and cytogenetics and soon to be Laboratory Genetics and Genomics program. I am also interested in developing curriculum to facilitate the training of clinical genetics professionals on new technology. Specifically I have been involved in developing tools that help counselors and clinicians to interpret new genetic technology such as microarray and Next Generation sequencing results for panels and exome sequencing. Since I am mostly involved in the clinical aspects of the Department of Human Genetics my research is collaborative where I provide a clinical perspective for others research programs. My goal is to provide clinical correlation for the basic science research projects in the department. I have been involved in projects looking at telomere genotype/phenotype correlations, Soto syndrome, and chromosome abnormalities. I have recently been involved in a project with Dr.Carole Ober studying different clinic phenotypes in the Hutterite populations.
One or more keywords matched the following items that are connected to Waggoner, Darrel J.
Item TypeName
Concept Chromosome Banding
Concept Chromosomes, Human, Pair 2
Concept Chromosomes, Human, Pair 6
Concept Chromosomes, Human, Pair 1
Concept Chromosome Deletion
Concept Chromosome Mapping
Concept Chromosomes, Human, Pair 4
Concept Chromosomes, Human, Pair 5
Concept Chromosomes, Human, Pair 10
Concept Chromosomes, Human, Pair 17
Concept Chromosomes, Human, Pair 19
Concept Sex Chromosome Aberrations
Concept X Chromosome Inactivation
Concept Chromosome Disorders
Concept Chromosome Aberrations
Concept Chromosomes
Concept Chromosomes, Human, Pair 16
Concept Chromosome Breakage
Concept Chromosomes, Human, X
Concept Chromosomes, Human, Y
Academic Article Partial monosomy of distal 10q: three new cases and a review.
Academic Article Deletion of 1q in a patient with acrofacial dysostosis.
Academic Article "Molecular rulers" for calibrating phenotypic effects of telomere imbalance.
Academic Article Genotype-phenotype associations in Sotos syndrome: an analysis of 266 individuals with NSD1 aberrations.
Academic Article Mechanisms of disease: epigenesis.
Academic Article Paternal deletion 6q24.3: a new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance.
Academic Article SMC1A expression and mechanism of pathogenicity in probands with X-Linked Cornelia de Lange syndrome.
Academic Article Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
Academic Article Mosaicism del(22)(q11.2q11.2)/dup(22)(q11.2q11.2) in a patient with features of 22q11.2 deletion syndrome.
Academic Article Microphthalmia with linear skin defects: a case report and review.
Academic Article Multiple mechanisms are implicated in the generation of 5q35 microdeletions in Sotos syndrome.
Academic Article Calibration of 6q subtelomere deletions to define genotype/phenotype correlations.
Academic Article Haploinsufficiency of TAB2 causes congenital heart defects in humans.
Academic Article Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13.
Academic Article A population-based study of autosomal-recessive disease-causing mutations in a founder population.
Academic Article Fine mapping of a locus for nonsyndromic mental retardation on chromosome 19p13.
Academic Article Evidence of a mechanism for isodicentric chromosome Y formation in a 45,X/46,X,idic(Y)(p11.31)/46,X,del(Y)(p11.31) mosaic karyotype.
Academic Article Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability.
Academic Article Expanding the spectrum of microdeletion 4q21 syndrome: a partial phenotype with incomplete deletion of the minimal critical region and a new association with cleft palate and Pierre Robin sequence.
Academic Article Reciprocal deletion and duplication at 2q23.1 indicates a role for MBD5 in autism spectrum disorder.
Academic Article 4q21 microdeletion in a patient with epilepsy and brain malformations.
Academic Article Chromosomal localization of CCS, the copper chaperone for Cu/Zn superoxide dismutase.
Academic Article Syndromic craniosynostosis associated with microdeletion of chromosome 19p13.12-19p13.2.
Academic Article The Effect of the Testis on the Ovary: Structure-Function Relationships in a Neonate with a Unilateral Ovotestis (Ovotesticular Disorder of Sex Development)?.
Academic Article Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Search Criteria
  • Chromosomes