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Alix Clemenson

Showing results (11-20 of 21) with videos related to

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Fertility and Sterility|July 22, 2010
Three-dimensional sonographic diagnosis of abdominal wall endometriosis: a useful tool?Anne Picard, Marie-Noelle Varlet, Francois Guillibert, et al.
Familial Cancer|November 21, 2019
MLH1 promoter hypermethylation: are you absolutely sure about the absence of MLH1 germline mutation? About a new caseCaroline Kientz, Fabienne Prieur, Alix Clemenson, et al.
The American Journal of Surgical Pathology|November 17, 2012
Conventional chondrosarcoma in a survivor of rhabdoid tumor: enlarging the spectrum of tumors associated with SMARCB1 germline mutationsFabien Forest, Audrey David, Sandrine Arrufat, et al.
Fetal Diagnosis and Therapy|February 5, 2003
Congenital diaphragmatic hernia. Two cases with early prenatal diagnosis and increased nuchal translucencyFrançois Varlet, Frantz Bousquet, Alix Clemenson, et al.
Hereditary Cancer in Clinical Practice|May 17, 2017
A case report of Muir-Torre syndrome in a woman with breast cancer and MSI-Low skin squamous cell carcinomaCaroline Kientz, Marie-Odile Joly, Laurence Faivre, et al.
Experimental and Molecular Pathology|November 28, 2017
EGFR, KRAS, BRAF and HER2 testing in metastatic lung adenocarcinoma: Value of testing on samples with poor specimen adequacy and analysis of discrepanciesFabien Forest, Marie-Laure Stachowicz, François Casteillo, et al.
Virchows Archiv : an International Journal of Pathology|July 4, 2019
Impact of delayed fixation and decalcification on PD-L1 expression: a comparison of two clonesFabien Forest, Gaelle Cote, David Laville, et al.
Prenatal Diagnosis|June 15, 2016
Fetal anomalies associated with HNF1B mutations: report of 20 autopsy casesHélène Duval, Laurence Michel-Calemard, Marie Gonzales, et al.
American Journal of Human Genetics|December 11, 2012
Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephalySandrine Vuillaumier-Barrot, Céline Bouchet-Séraphin, Malika Chelbi, et al.
Clinical Genetics|July 5, 2020
Fetal megacystis-microcolon: Genetic mutational spectrum and identification of PDCL3 as a novel candidate geneClarisse Billon, Arnaud Molin, Céline Poirsier, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Fertility and Sterility|July 22, 2010
Three-dimensional sonographic diagnosis of abdominal wall endometriosis: a useful tool?Anne Picard, Marie-Noelle Varlet, Francois Guillibert, et al.
Familial Cancer|November 21, 2019
MLH1 promoter hypermethylation: are you absolutely sure about the absence of MLH1 germline mutation? About a new caseCaroline Kientz, Fabienne Prieur, Alix Clemenson, et al.
The American Journal of Surgical Pathology|November 17, 2012
Conventional chondrosarcoma in a survivor of rhabdoid tumor: enlarging the spectrum of tumors associated with SMARCB1 germline mutationsFabien Forest, Audrey David, Sandrine Arrufat, et al.
Fetal Diagnosis and Therapy|February 5, 2003
Congenital diaphragmatic hernia. Two cases with early prenatal diagnosis and increased nuchal translucencyFrançois Varlet, Frantz Bousquet, Alix Clemenson, et al.
Hereditary Cancer in Clinical Practice|May 17, 2017
A case report of Muir-Torre syndrome in a woman with breast cancer and MSI-Low skin squamous cell carcinomaCaroline Kientz, Marie-Odile Joly, Laurence Faivre, et al.
Experimental and Molecular Pathology|November 28, 2017
EGFR, KRAS, BRAF and HER2 testing in metastatic lung adenocarcinoma: Value of testing on samples with poor specimen adequacy and analysis of discrepanciesFabien Forest, Marie-Laure Stachowicz, François Casteillo, et al.
Virchows Archiv : an International Journal of Pathology|July 4, 2019
Impact of delayed fixation and decalcification on PD-L1 expression: a comparison of two clonesFabien Forest, Gaelle Cote, David Laville, et al.
Prenatal Diagnosis|June 15, 2016
Fetal anomalies associated with HNF1B mutations: report of 20 autopsy casesHélène Duval, Laurence Michel-Calemard, Marie Gonzales, et al.
American Journal of Human Genetics|December 11, 2012
Identification of mutations in TMEM5 and ISPD as a cause of severe cobblestone lissencephalySandrine Vuillaumier-Barrot, Céline Bouchet-Séraphin, Malika Chelbi, et al.
Clinical Genetics|July 5, 2020
Fetal megacystis-microcolon: Genetic mutational spectrum and identification of PDCL3 as a novel candidate geneClarisse Billon, Arnaud Molin, Céline Poirsier, et al.
Pageof 3