Laurent Fasano

5PUBLICATIONS
13CO-AUTHORS
Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Separation technologiesNeurogenetics
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Publications (5)

|Oct 17, 2024
Heterozygous variants in the teashirt zinc finger homeobox 3 (TSHZ3) gene in human congenital anomalies of the kidney and urinary tract.

Esra Kesdiren, Helge Martens, Frank Brand

|May 23, 2022
Correction: Targeted Tshz3 deletion in corticostriatal circuit components segregates core autistic behaviors.

Xavier Caubit, Paolo Gubellini, Pierre L Roubertoux

|Mar 16, 2022
Targeted Tshz3 deletion in corticostriatal circuit components segregates core autistic behaviors.

Xavier Caubit, Paolo Gubellini, Pierre L Roubertoux

|Dec 17, 2021
Haploinsufficiency of the mouse Tshz3 gene leads to kidney defects.

Irene Sanchez-Martin, Pedro Magalhães, Parisa Ranjzad

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