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Bertrand Isidor

Showing results (1-10 of 365) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2022
Response to Kossmann Ferraz et alMathilde Nizon, Bertrand Isidor
European Journal of Medical Genetics|December 3, 2014
Two girls with short stature, short neck, vertebral anomalies, Sprengel deformity and intellectual disabilityBertrand Isidor, Albert David
Medecine Sciences : M/S|April 23, 2024
[Exome, genome and incidental findings]Jeanne Amiel, Delphine Héron, Bertrand Isidor
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 12, 2017
Familial deep endometriosis: A rare monogenic disease?Bertrand Isidor, Xenia Latypova, Stéphane Ploteau
Medecine Sciences : M/S|December 5, 2017
[Should the knowledge be imperative? The key challenge of high throughput genetics]Bertrand Isidor, Sophie Julia, Mathilde Nizon, et al.
European Journal of Medical Genetics|February 26, 2021
Letter regarding the article "two girls with short stature, short neck, vertebral anomalies, Sprengel deformity and intellectual disability" (Isidor et al., 2015)Xenia Latypova, Xiao Dang, Jianguo Zhang, et al.
European Journal of Medical Genetics|September 13, 2022
Challenges of preconception genetic testing in France: A qualitative studyEugénie Hoarau, Xenia Latypova, Maud Jourdain, et al.
Neurogenetics|September 25, 2012
Refining the phenotype associated with MEF2C point mutationsThierry Bienvenu, Bertrand Diebold, Jamel Chelly, et al.
Neurogenetics|June 1, 2023
Response to a letter to the editorJeanne Jury, Mathilde Nizon, Benjamin Cogné, et al.
Nephrologie & Therapeutique|February 1, 2022
[Genetic screening is essential in polycystic kidney disease: It is never too late!]Clémence Petit, Diego Cantarovich, Virginie Langs, et al.
Pageof 37

Showing results (1-10 of 365) with videos related to

Sort By:
Pageof 37
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 3, 2022
Response to Kossmann Ferraz et alMathilde Nizon, Bertrand Isidor
European Journal of Medical Genetics|December 3, 2014
Two girls with short stature, short neck, vertebral anomalies, Sprengel deformity and intellectual disabilityBertrand Isidor, Albert David
Medecine Sciences : M/S|April 23, 2024
[Exome, genome and incidental findings]Jeanne Amiel, Delphine Héron, Bertrand Isidor
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 12, 2017
Familial deep endometriosis: A rare monogenic disease?Bertrand Isidor, Xenia Latypova, Stéphane Ploteau
Medecine Sciences : M/S|December 5, 2017
[Should the knowledge be imperative? The key challenge of high throughput genetics]Bertrand Isidor, Sophie Julia, Mathilde Nizon, et al.
European Journal of Medical Genetics|February 26, 2021
Letter regarding the article "two girls with short stature, short neck, vertebral anomalies, Sprengel deformity and intellectual disability" (Isidor et al., 2015)Xenia Latypova, Xiao Dang, Jianguo Zhang, et al.
European Journal of Medical Genetics|September 13, 2022
Challenges of preconception genetic testing in France: A qualitative studyEugénie Hoarau, Xenia Latypova, Maud Jourdain, et al.
Neurogenetics|September 25, 2012
Refining the phenotype associated with MEF2C point mutationsThierry Bienvenu, Bertrand Diebold, Jamel Chelly, et al.
Neurogenetics|June 1, 2023
Response to a letter to the editorJeanne Jury, Mathilde Nizon, Benjamin Cogné, et al.
Nephrologie & Therapeutique|February 1, 2022
[Genetic screening is essential in polycystic kidney disease: It is never too late!]Clémence Petit, Diego Cantarovich, Virginie Langs, et al.
Pageof 37