Assistant Professor, Medicine, University of Chicago Div of the Bio Sci The Pritzker SOM

Medical Genetics

Dr. Gordana Raca, MD

Gordana Raca, MD is an expert in the field of Medical Genetics. Dr. Gordana Raca is also published. She has 22 publications published. The lastest publication: "Trinucleotide repeats affect DNA replication in vivo.'

Publications

MECP2 duplication: Possible cause of severe phenotype in females.
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.
Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridization.
Phenotype of FOXP2 haploinsufficiency in a mother and son.
DNA methylation assay for X-chromosome inactivation in female human iPS cells.
Array comparative genomic hybridization analysis in patients with anophthalmia, microphthalmia, and coloboma.
Chromosomal abnormalities in 2 cases of testicular failure.
Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism.
Next generation sequencing in research and diagnostics of ocular birth defects.
Clinical and molecular characterization of overlapping interstitial Xp21-p22 duplications in two unrelated individuals.
Array-based comparative genomic hybridization (aCGH) in the genetic evaluation of stillbirth.
Mild clinical presentation in a child with prenatally diagnosed 45,X/47,XX,+18 mosaicism.
Detailed characterization of, and clinical correlations in, 10 patients with distal deletions of chromosome 9p.
Paternal deletion 6q24.3: a new congenital anomaly syndrome associated with intrauterine growth failure, early developmental delay and characteristic facial appearance.
Intrachromosomal duplications of 22q11 are not a common cause of isolated coloboma and coloboma with other limited features of cat eye syndrome.
NSD1 analysis for Sotos syndrome: insights and perspectives from the clinical laboratory.
Deletion analysis of the imprinting center region in patients with Angelman syndrome and Prader-Willi syndrome by real-time quantitative PCR.
Progressive dystonia in a 12-year-old boy.
Expansion of the (CTG)(n) repeat in the 5''-UTR of a reporter gene impedes translation.
Trinucleotide repeats affect DNA replication in vivo.
The advantage of using SNP array in clinical testing for hematological malignancies-a comparative study of three genetic testing methods.

Doctors Specialties

Clinical Cytogenetics
Clinical Molecular Genetics
Medical Genetics

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