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Publications by C Ferec

A Mutation in Exon 7 of the CFTR Gene Is Common in the Western Part of France.

Journal of Medical Genetics

Genetics

1992

English

Related publications

A 2-Base Insertion in Exon 5 Is a Common Mutation of the TP53 Gene in Dogs With Histiocytic Sarcoma

Journal of Veterinary Medical Science

Veterinary

2017

English

The Exon a (C77G) Mutation Is a Common Cause of Abnormal CD45 Splicing in Humans

Journal of Immunology

Allergy

Immunology

2001

English

Severe Cystic Fibrosis in a Child Homozygous for the G542 Nonsense Mutation in the CFTR Gene.

Journal of Medical Genetics

Genetics

1993

English

Mutation in Exon 13 of the TCOF1 Gene in Patient With Treacher Collins Syndrome

Acta Fytotechnica et Zootechnica

English

Primary Hyperoxaluria Type 1: A Cluster of New Mutations in Exon 7 of the AGXT Gene.

Journal of Medical Genetics

Genetics

1997

English

A New Complex Allele of the CFTR Gene Partially Explains the Variable Phenotype of the L997F Mutation

English

Clinical Hallmarks and Genetic Polymorphisms in the CFTR Gene Contribute to the Disclosure of the A1006E Mutation

Clinical and Investigative Medicine

Medicine

2010

English

A Common Founder Mutation in the EDA-A1 Gene in X-Linked Hypodontia

Dermatology

2010

English

Compound Heterozygosity of a Novel Exon 3 Frameshift (p.R357P Fs*24) Mutation and Y486D Mutation in Exon 5 of the UGT1A1 Gene in a Thai Infant With Crigler-Najjar Syndrome Type 2

Genetics and Molecular Research

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by C Ferec

A Mutation in Exon 7 of the CFTR Gene Is Common in the Western Part of France.

Related publications

A 2-Base Insertion in Exon 5 Is a Common Mutation of the TP53 Gene in Dogs With Histiocytic Sarcoma

The Exon a (C77G) Mutation Is a Common Cause of Abnormal CD45 Splicing in Humans

Severe Cystic Fibrosis in a Child Homozygous for the G542 Nonsense Mutation in the CFTR Gene.

Mutation in Exon 13 of the TCOF1 Gene in Patient With Treacher Collins Syndrome

Primary Hyperoxaluria Type 1: A Cluster of New Mutations in Exon 7 of the AGXT Gene.

A New Complex Allele of the CFTR Gene Partially Explains the Variable Phenotype of the L997F Mutation

Clinical Hallmarks and Genetic Polymorphisms in the CFTR Gene Contribute to the Disclosure of the A1006E Mutation

A Common Founder Mutation in the EDA-A1 Gene in X-Linked Hypodontia

Compound Heterozygosity of a Novel Exon 3 Frameshift (p.R357P Fs*24) Mutation and Y486D Mutation in Exon 5 of the UGT1A1 Gene in a Thai Infant With Crigler-Najjar Syndrome Type 2