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Elsa Excoffier

Research Profile

Disorders

Anatomy

Chromosomes, Human, Pair 22

Occupations

Genetic Counseling

Concepts & Ideas

Procedures

Fluorescence In Situ Hybridization

Activities & Behaviors

Geographic Areas

France

Physiology

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Co-author Network

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Publications

TOP 3
Elsa Excoffier; Gilbert Vila; Emmanuelle Taupiac; Marie-Christine Mouren-Simeoni; Manuel Bouvard
[Dimensional approach of social behaviour deficits in children. Preliminary validation study of the French version of the Children's Social Behaviour Questionnaire (CSBQ)].
David Cohen; Nadège Pichard; Sylvie Tordjman; Clarisse Baumann; Lydie Burglen; Elsa Excoffier; Gabriela Lazar; Philippe Mazet; Clément Pinquier; Alain Verloes; Delphine Héron
Specific genetic disorders and autism: clinical contribution towards their identification.
Cyril Goizet; Elsa Excoffier; Laurence Taine; Emmanuelle Taupiac; A A El Moneim; Benoît Arveiler; Manuel Bouvard; Didier Lacombe
Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH.

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All Publications

2007: Elsa Excoffier; Gilbert Vila; Emmanuelle Taupiac; Marie-Christine Mouren-Simeoni; Manuel Bouvard
[Dimensional approach of social behaviour deficits in children. Preliminary validation study of the French version of the Children's Social Behaviour Questionnaire (CSBQ)].
L'Encéphale 2007;33(4 Pt 1):585-91.
2005: David Cohen; Nadège Pichard; Sylvie Tordjman; Clarisse Baumann; Lydie Burglen; Elsa Excoffier; Gabriela Lazar; Philippe Mazet; Clément Pinquier; Alain Verloes; Delphine Héron
Specific genetic disorders and autism: clinical contribution towards their identification.
Journal of autism and developmental disorders 2005;35(1):103-16.
2000: Cyril Goizet; Elsa Excoffier; Laurence Taine; Emmanuelle Taupiac; A A El Moneim; Benoît Arveiler; Manuel Bouvard; Didier Lacombe
Case with autistic syndrome and chromosome 22q13.3 deletion detected by FISH.
American journal of medical genetics 2000;96(6):839-44.

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