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Catherine Vincent

Showing results (91-100 of 188) with videos related to

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Chemical Science|December 18, 2024
A reliable, colloidal synthesis method of the orthorhombic chalcogenide perovskite, BaZrS<sub>3</sub>, and related ABS<sub>3</sub> nanomaterials (A = Sr, Ba; B = Ti, Zr, Hf): a step forward for earth-abundant, functional materialsDaniel C Hayes, Shubhanshu Agarwal, Kiruba Catherine Vincent, et al.
European Journal of Human Genetics : EJHG|December 2, 2022
Correction to: Evaluation of somatic and/or germline mosaicism in congenital malformation of the eyeBertrand Chesneau, Véronique Ivashchenko, Christophe Habib, et al.
Gynecologic Oncology|July 19, 2005
Performance of the Roche AMPLICOR human papillomavirus (HPV) test in prediction of cervical intraepithelial neoplasia (CIN) in women with abnormal PAP smearJoseph Monsonego, Jean Marc Bohbot, Giuseppe Pollini, et al.
Neurogenetics|September 20, 2015
Recurrent KIF5C mutation leading to frontal pachygyria without microcephalyMara Cavallin, Laurence Hubert, Vincent Cantagrel, et al.
European Journal of Medical Genetics|April 11, 2015
Microduplications of 3p26.3p26.2 containing CRBN gene in patients with intellectual disability and behavior abnormalitiesSorina M Papuc, Karl Hackmann, Joris Andrieux, et al.
European Journal of Human Genetics : EJHG|November 20, 2022
Evaluation of somatic and/or germline mosaicism in congenital malformation of the eyeBertrand Chesneau, Véronique Ivashchenko, Christophe Habib, et al.
Canadian Liver Journal|July 18, 2025
Evolving trends in liver transplantation eligibility: A shift toward inclusivity for older adults at a Canadian Transplant CenterGabrielle Jutras, Genevieve Huard, Marc Bilodeau, et al.
European Journal of Medical Genetics|December 21, 2024
NONO-related X-linked intellectual disability syndrome: Further clinical and molecular delineationPauline Planté-Bordeneuve, Simon Boussion, Roseline Caumes, et al.
American Journal of Medical Genetics. Part A|April 12, 2017
WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletionMinh Tuan Huynh, Elise Boudry-Labis, Bénédicte Duban, et al.
European Journal of Heart Failure|March 7, 2006
Clinical profile, contemporary management and one-year mortality in patients with severe acute heart failure syndromes: The EFICA studyFaiez Zannad, Alexandre Mebazaa, Yves Juillière, et al.
Pageof 19

Showing results (91-100 of 188) with videos related to

Sort By:
Pageof 19
Chemical Science|December 18, 2024
A reliable, colloidal synthesis method of the orthorhombic chalcogenide perovskite, BaZrS<sub>3</sub>, and related ABS<sub>3</sub> nanomaterials (A = Sr, Ba; B = Ti, Zr, Hf): a step forward for earth-abundant, functional materialsDaniel C Hayes, Shubhanshu Agarwal, Kiruba Catherine Vincent, et al.
European Journal of Human Genetics : EJHG|December 2, 2022
Correction to: Evaluation of somatic and/or germline mosaicism in congenital malformation of the eyeBertrand Chesneau, Véronique Ivashchenko, Christophe Habib, et al.
Gynecologic Oncology|July 19, 2005
Performance of the Roche AMPLICOR human papillomavirus (HPV) test in prediction of cervical intraepithelial neoplasia (CIN) in women with abnormal PAP smearJoseph Monsonego, Jean Marc Bohbot, Giuseppe Pollini, et al.
Neurogenetics|September 20, 2015
Recurrent KIF5C mutation leading to frontal pachygyria without microcephalyMara Cavallin, Laurence Hubert, Vincent Cantagrel, et al.
European Journal of Medical Genetics|April 11, 2015
Microduplications of 3p26.3p26.2 containing CRBN gene in patients with intellectual disability and behavior abnormalitiesSorina M Papuc, Karl Hackmann, Joris Andrieux, et al.
European Journal of Human Genetics : EJHG|November 20, 2022
Evaluation of somatic and/or germline mosaicism in congenital malformation of the eyeBertrand Chesneau, Véronique Ivashchenko, Christophe Habib, et al.
Canadian Liver Journal|July 18, 2025
Evolving trends in liver transplantation eligibility: A shift toward inclusivity for older adults at a Canadian Transplant CenterGabrielle Jutras, Genevieve Huard, Marc Bilodeau, et al.
European Journal of Medical Genetics|December 21, 2024
NONO-related X-linked intellectual disability syndrome: Further clinical and molecular delineationPauline Planté-Bordeneuve, Simon Boussion, Roseline Caumes, et al.
American Journal of Medical Genetics. Part A|April 12, 2017
WAGR syndrome and congenital hypothyroidism in a child with a Mosaic 11p13 deletionMinh Tuan Huynh, Elise Boudry-Labis, Bénédicte Duban, et al.
European Journal of Heart Failure|March 7, 2006
Clinical profile, contemporary management and one-year mortality in patients with severe acute heart failure syndromes: The EFICA studyFaiez Zannad, Alexandre Mebazaa, Yves Juillière, et al.
Pageof 19