Chambon Pascal - Dept Cytogenet, Univ Rouen

基本信息

浏览量：1

职业迁徙

个人简介

暂无内容

研究兴趣

论文共 36 篇作者统计合作学者相似作者

按年份排序按引用量排序主题筛选期刊级别筛选合作者筛选合作机构筛选

Cat Eye Syndrome: Clinical, Cytogenetics and Familial Findings in a Large Cohort of 43 Patients Highlighting the Importance of Congenital Heart Disease and Inherited Cases

Guillaume Jedraszak,Florence Jobic,Aline Receveur,Frederic Bilan,Brigitte Gilbert-Dussardier,Busa Tiffany,Chantal Missirian,Marjolaine Willems,Sylvie Odent,Josette Lucas,Christele Dubourg,Elise Schaefer,

AMERICAN JOURNAL OF MEDICAL GENETICS PART Ano. 4 (2024)

引用0浏览0WOS引用

Evidence for High Breakpoint Variability in 46, XX, SRY‐positive Testicular Disorder and Frequent ARSE Deletion That May Be Associated with Short Stature

Celine Capron,Louis Januel,Gaelle Vieville,Sylvie Jaillard,Paul Kuentz,Gaelle Salaun,Gwenael Nadeau,Patrice Clement,Marie Pierre Brechard,Berenice Herve,Jean Michel Dupont,Nicolas Gruchy,

Andrology (2022): 1625-1631

引用1浏览0WOS引用

Heterozygous Deletion of the VEGFC Gene in 4q34.3 is Associated with Milroy-Like Lymphedema: First Prenatal Case Report

Minh-Tuan Huynh,Sophie Degre,Geraldine Joly-Helas,Cathy Breon, Stephanie Potel,Pascal Chambon,Jerome Bouligand,Valerie Layet

American journal of medical genetics Part A（2022）

引用1浏览0WOS引用

Large genomic imbalances and phenotype

Martine Doco-Fenzy,Jean Michel Dupont,Chantal Missirian,Patrick Callier,Valerie Malan,Sylvia Redon,Emilie Landais,Lucas Herissant,Paul Kuentz,Gaelle Vieville,Marie Faoucher,Olivier Pichon,

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

引用0浏览0引用

Detection of Copy-Number Variations from NGS Data Using Read Depth Information: a Diagnostic Performance Evaluation

Olivier Quenez,Kevin Cassinari,Sophie Coutant,Francois Lecoquierre,Kilan Le Guennec,Stephane Rousseau,Anne-Claire Richard,Stephanie Vasseur,Emilie Bouvignies,Jacqueline Bou,Gwendoline Lienard,Sandrine Manase,

EUROPEAN JOURNAL OF HUMAN GENETICS（2021）

引用21浏览0引用

A, Not So Robertsonian, Translocation

Julie Amiot,Valérie Layet, Alain Talbot,Mathieu Castelain,Thierry Frebourg,Pascal Chambon,Nathalie Le Meur, Géraldine Joly Helas,Kévin Cassinari

ANNALES DE BIOLOGIE CLINIQUE（2021）

引用0浏览0WOS引用

Neuropathological Hallmarks of Fetal Hydrocephalus Linked to CCDC88C Pathogenic Variants

Marguet Florent,Vezain Myriam,Marcorelles Pascale,Audebert-Bellanger Séverine,Cassinari Kévin,Drouot Nathalie,Chambon Pascal,Gonzalez Bruno J.,Horowitz Arie, Pathology Laboratory, Pavillon Jacques Delarue,Saugier-Veber Pascale

Acta neuropathologica communications（2021）

引用4浏览0WOS引用

Recurrence of an Early Postzygotic Rescue of an Inherited Unbalanced Translocation Resulting in Mosaic Segmental Uniparental Isodisomy of Chromosome 11q in Siblings

Maud Blanluet,Sandra Chantot-Bastaraud,Pascal Chambon,Kevin Cassinari,Gabriella Vera,Alice Goldenberg,Boris Keren,Nathalie Le Meur,Didier Hannequin,Bertrand Mace,Jean-Pierre Siffroi,Thierry Frebourg,

American journal of medical genetics Part Ano. 10 (2021): 3057-3061

引用1浏览0WOS引用

Assessment of Multiplex Digital Droplet RT-PCR As a Diagnostic Tool for SARS-CoV-2 Detection in Nasopharyngeal Swabs and Saliva Samples

Kevin Cassinari,Elodie Alessandri-Gradt,Pascal Chambon,Francoise Charbonnier,Segolene Gracias,Ludivine Beaussire,Kevin Alexandre,Nasrin Sarafan-Vasseur,Claude Houdayer,Manuel Etienne,Francois Caron,Jean Christophe Plantier,

Clinical chemistry（2021）

引用26浏览0WOS引用

Patients with 10q22.3q23.1 Recurrent Deletion Syndrome Are at Risk for Juvenile Polyposis

Francois Lecoquierre,Kevin Cassinari,Pascal Chambon,Gael Nicolas,Sarah Malsa,Regine Marlin, Yvon Assouline,Jean-Francois Flejou,Thierry Frebourg,Claude Houdayer,Odile Bera,Stephanie Baert-Desurmont

European journal of medical genetics（2020）

引用4浏览0WOS引用

加载更多

作者统计

合作学者

合作机构

D-Core

合作者
学生
导师

暂无相似学者，你可以通过学者研究领域进行搜索筛选

数据免责声明

页面数据均来自互联网公开来源、合作出版商和通过AI技术自动分析结果，我们不对页面数据的有效性、准确性、正确性、可靠性、完整性和及时性做出任何承诺和保证。若有疑问，可以通过电子邮件方式联系我们：report@aminer.cn