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Viot

Showing results (141-150 of 228) with videos related to

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L'Encephale|June 16, 2001
[French validation of a Minor Morphologic Anomalies Scale in schizophrenic patients and their parents]D Gourion, G Viot, C Goldberger, et al.
Psychiatry Research|February 28, 2012
Atypical presentations of 22q11.2 deletion syndrome: explaining the genetic defects and genome architectureAndreea Cristina Tuţulan-Cuniţă, Magdalena Budişteanu, Sorina Mihaela Papuc, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndromeV Cormier-Daire, V Belin, V Cusin, et al.
American Journal of Medical Genetics. Part A|July 22, 2004
Atypical findings in Kabuki syndrome: report of 8 patients in a series of 20 and review of the literatureD Geneviève, J Amiel, G Viot, et al.
Nature Genetics|May 20, 1998
SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)V Belin, V Cusin, G Viot, et al.
Gastroenterologie Clinique Et Biologique|March 28, 2006
Hepatitis B vaccination in HIV-infected patients: a survey of physicians and patients participating in the Aquitaine cohortMaria Winnock, Didier Neau, Laurent Castera, et al.
The Journal of Antimicrobial Chemotherapy|November 18, 1998
Cefepime versus imipenem-cilastatin as empirical monotherapy in 400 febrile patients with short duration neutropenia. CEMIC (Study Group of Infectious Diseases in Cancer)P Biron, C Fuhrmann, H Cure, et al.
Environmental Research|June 21, 2020
Cancer incidence in the vicinity of a waste incineration plant in the Nice area between 2005 and 2014Eugènia Mariné Barjoan, Nadège Doulet, Amel Chaarana, et al.
Clinical Genetics|July 3, 1998
Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndromeG Viot-Szoboszlai, J Amiel, F Doz, et al.
Genome Biology|October 10, 2024
Transipedia.org: k-mer-based exploration of large RNA sequencing datasets and application to cancer dataChloé Bessière, Haoliang Xue, Benoit Guibert, et al.
Pageof 23

Showing results (141-150 of 228) with videos related to

Sort By:
Pageof 23
L'Encephale|June 16, 2001
[French validation of a Minor Morphologic Anomalies Scale in schizophrenic patients and their parents]D Gourion, G Viot, C Goldberger, et al.
Psychiatry Research|February 28, 2012
Atypical presentations of 22q11.2 deletion syndrome: explaining the genetic defects and genome architectureAndreea Cristina Tuţulan-Cuniţă, Magdalena Budişteanu, Sorina Mihaela Papuc, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
SHOX gene mutations and deletions in dyschondrosteosis or Leri-Weill syndromeV Cormier-Daire, V Belin, V Cusin, et al.
American Journal of Medical Genetics. Part A|July 22, 2004
Atypical findings in Kabuki syndrome: report of 8 patients in a series of 20 and review of the literatureD Geneviève, J Amiel, G Viot, et al.
Nature Genetics|May 20, 1998
SHOX mutations in dyschondrosteosis (Leri-Weill syndrome)V Belin, V Cusin, G Viot, et al.
Gastroenterologie Clinique Et Biologique|March 28, 2006
Hepatitis B vaccination in HIV-infected patients: a survey of physicians and patients participating in the Aquitaine cohortMaria Winnock, Didier Neau, Laurent Castera, et al.
The Journal of Antimicrobial Chemotherapy|November 18, 1998
Cefepime versus imipenem-cilastatin as empirical monotherapy in 400 febrile patients with short duration neutropenia. CEMIC (Study Group of Infectious Diseases in Cancer)P Biron, C Fuhrmann, H Cure, et al.
Environmental Research|June 21, 2020
Cancer incidence in the vicinity of a waste incineration plant in the Nice area between 2005 and 2014Eugènia Mariné Barjoan, Nadège Doulet, Amel Chaarana, et al.
Clinical Genetics|July 3, 1998
Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndromeG Viot-Szoboszlai, J Amiel, F Doz, et al.
Genome Biology|October 10, 2024
Transipedia.org: k-mer-based exploration of large RNA sequencing datasets and application to cancer dataChloé Bessière, Haoliang Xue, Benoit Guibert, et al.
Pageof 23