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Patricia Blanchet

Research Profile

Chemicals & Drugs

Disorders

Physiology

Procedures

Geographic Areas

France

Anatomy

Chromosomes, Human, Pair 22

Genes & Molecular Sequences

Recessive Genes

Concepts & Ideas

Gene Frequency

Activities & Behaviors

Cost Benefit Analysis

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Publications

TOP 3
Anne-Françoise Roux; Nathalie Pallares-Ruiz; Anne Vielle; Valérie Faugère; Carine Templin; Dorothée Leprevost; Françoise Artières; Geneviève Lina; Nicolas Molinari; Patricia Blanchet; Michel Mondain; Mireille Claustres
Molecular epidemiology of DFNB1 deafness in France.
Frédéric Venail; Anne-Françoise Roux; Nathalie Pallares-Ruiz; Mireille Claustres; Patricia Blanchet; Quentin Gardiner; Michel Mondain
Nonsyndromic 35 delG mutation of the connexin 26 gene associated with deafness in syndromic children: two case reports.
Nathalie Pallares-Ruiz; Patricia Blanchet; Michel Mondain; Mireille Claustres; Anne-Françoise Roux
A large deletion including most of GJB6 in recessive non syndromic deafness: a digenic effect?

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All Publications

2004: Anne-Françoise Roux; Nathalie Pallares-Ruiz; Anne Vielle; Valérie Faugère; Carine Templin; Dorothée Leprevost; Françoise Artières; Geneviève Lina; Nicolas Molinari; Patricia Blanchet; Michel Mondain; Mireille Claustres
Molecular epidemiology of DFNB1 deafness in France.
BMC medical genetics 2004;5():5.
2004: Frédéric Venail; Anne-Françoise Roux; Nathalie Pallares-Ruiz; Mireille Claustres; Patricia Blanchet; Quentin Gardiner; Michel Mondain
Nonsyndromic 35 delG mutation of the connexin 26 gene associated with deafness in syndromic children: two case reports.
The Laryngoscope 2004;114(3):566-9.
2002: Nathalie Pallares-Ruiz; Patricia Blanchet; Michel Mondain; Mireille Claustres; Anne-Françoise Roux
A large deletion including most of GJB6 in recessive non syndromic deafness: a digenic effect?
European journal of human genetics : EJHG 2002;10(1):72-6.
2001: Nathalie Pallares-Ruiz; Patricia Blanchet; Michel Mondain; S Low-Hong; Jacques Demaille; Mireille Claustres; Anne-Françoise Roux
Evaluation of dHPLC for CX26 mutation screening in patients from southern France with sensorineural deafness.
Genetic testing 2001;5(4):339-43.

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