Kimberly N. Forlenza
Obstetrics and Gynecology
10652 Wrigley Field Ave
Denham Springs, LA 70726
Denham Springs, LA 70726
Last Updated: 09/26/2026
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Found 7 publications
Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathies.
Journal: Human mutation
Published: July 03, 2017
Mutations in DYNC2H1, the cytoplasmic dynein 2, heavy chain 1 motor protein gene, cause short-rib polydactyly type I, Saldino-Noonan type.
Journal: Clinical genetics
Published: August 22, 2016
A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis.
Journal: Scientific reports
Published: August 12, 2016
An inactivating mutation in intestinal cell kinase, ICK, impairs hedgehog signalling and causes short rib-polydactyly syndrome.
Journal: Human molecular genetics
Published: June 27, 2016
Destabilization of the IFT-B cilia core complex due to mutations in IFT81 causes a Spectrum of Short-Rib Polydactyly Syndrome.
Journal: Scientific reports
Published: June 01, 2016
TGFβ and BMP Dependent Cell Fate Changes Due to Loss of Filamin B Produces Disc Degeneration and Progressive Vertebral Fusions.
Journal: PLoS genetics
Published: August 25, 2015
Showing 1-7 of 7
Last Updated: 09/26/2026