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Laure Lecerf

Showing results (11-20 of 15) with videos related to

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Science Advances|November 12, 2025
Glial-to-mesenchymal transition of tumor Schwann cells drives the genetic burden in MPNSTs from neurofibromatosis type 1 mouse modelKatarzyna J Radomska, Audrey Onfroy, Laure Lecerf, et al.
European Journal of Human Genetics : EJHG|April 29, 2010
Recurrent 70.8 Mb 4q22.2q32.3 duplication due to ovarian germinal mosaicismLucie Tosca, Sophie Brisset, François M Petit, et al.
American Journal of Medical Genetics. Part A|June 26, 2010
Syndromic mental retardation with thrombocytopenia due to 21q22.11q22.12 deletion: Report of three patientsEleni Katzaki, Gilles Morin, Marzia Pollazzon, et al.
Molecular Genetics & Genomic Medicine|September 28, 2021
Two new cases of interstitial 7q35q36.1 deletion including CNTNAP2 and KMT2CLucie Tosca, Loïc Drévillon, Aurélie Mouka, et al.
Cancer Research|December 18, 2003
FGFR3 and TP53 gene mutations define two distinct pathways in urothelial cell carcinoma of the bladderAshraf A Bakkar, Herve Wallerand, François Radvanyi, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Science Advances|November 12, 2025
Glial-to-mesenchymal transition of tumor Schwann cells drives the genetic burden in MPNSTs from neurofibromatosis type 1 mouse modelKatarzyna J Radomska, Audrey Onfroy, Laure Lecerf, et al.
European Journal of Human Genetics : EJHG|April 29, 2010
Recurrent 70.8 Mb 4q22.2q32.3 duplication due to ovarian germinal mosaicismLucie Tosca, Sophie Brisset, François M Petit, et al.
American Journal of Medical Genetics. Part A|June 26, 2010
Syndromic mental retardation with thrombocytopenia due to 21q22.11q22.12 deletion: Report of three patientsEleni Katzaki, Gilles Morin, Marzia Pollazzon, et al.
Molecular Genetics & Genomic Medicine|September 28, 2021
Two new cases of interstitial 7q35q36.1 deletion including CNTNAP2 and KMT2CLucie Tosca, Loïc Drévillon, Aurélie Mouka, et al.
Cancer Research|December 18, 2003
FGFR3 and TP53 gene mutations define two distinct pathways in urothelial cell carcinoma of the bladderAshraf A Bakkar, Herve Wallerand, François Radvanyi, et al.
Pageof 2