Dr. Jerome L Gorski MD
Pediatrician
402 N Keene St Suite 101 Columbia MO, 65201Rating
3/5
About
Dr. Jerome Gorski is a pediatrician practicing in Columbia, MO. Dr. Gorski is a doctor who specializes in the health care of children. As a pedicatrician, Dr. Gorski 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. Gorski can oversee and manage the physical, mental and emotional health of their patients.
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologues.
- Isolation, characterization, and mapping of the mouse Fgd3 gene, a new
- Skeletal-specific expression of Fgd1 during bone formation and skeletal defects in faciogenital dysplasia (FGDY; Aarskog syndrome).
- In memoriam: James V. Neel, 1915-2000.
- Fgd1, the Cdc42 guanine nucleotide exchange factor responsible for faciogenital dysplasia, is localized to the subcortical actin cytoskeleton and Golgi membrane.
- CHARGE association with choanal atresia and inner ear hypoplasia in a child with a de novo chromosome translocation t(2;7)(p14;q21.11).
- Retinitis pigmentosa, growth hormone deficiency, and acromelic skeletal dysplasia in two brothers: possible familial RHYNS syndrome.
- Ocular malformations, postaxial polydactyly, and delayed intramembranous ossification: a new autosomal dominant condition.
- The Caenorhabditis elegans homolog of FGD1, the human Cdc42 GEF gene responsible for faciogenital dysplasia, is critical for excretory cell morphogenesis.
- Interrupted aortic arch in a child with trisomy 5q31.1q35.1 due to a maternal (20;5) balanced insertion.
- Acute extrapyramidal syndrome in mild ornithine transcarbamylase deficiency: metabolic stroke involving the caudate and putamen without metabolic decompensation.
- Fgd1, the Cdc42 GEF responsible for Faciogenital Dysplasia, directly interacts with cortactin and mAbp1 to modulate cell shape.
- Isolation of DNA markers from a region between incontinentia pigmenti 1 (IP1) X-chromosomal translocation breakpoints by a comparative PCR analysis of a radiation hybrid subclone mapping panel.
- A radiation hybrid map of the proximal short arm of the human X chromosome spanning incontinentia pigmenti 1 (IP1) translocation breakpoints.
- Oculo-facio-cardio-dental syndrome: skewed X chromosome inactivation in mother and daughter suggest X-linked dominant Inheritance.
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Nearby Providers
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Dr. John Pardalos MD404 N Keene St Columbia MO 65201![]()
Dr. Sayonara Mato MD, MPH&TMOne Hospital Drive Columbia MO 65212![]()
Dr. Tina Brockman MD201 W BROADWAY COLUMBIA MO 65203![]()
Dr. Tracy A Stroud DO404 N Keene St Columbia MO 65201![]()
Dr. Michael J Gardner MD1 Hospital Dr Columbia MO 65212![]()
Dr. Justin T Hagen D.O.404 N Keene Street Columbia MO 65201
Nearest Hospitals
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