First Report of Three Cystic Fibrosis Patients Homozygous for the 1717-1g-->A Mutation.

Journal of Medical Genetics - United Kingdom
doi 10.1136/jmg.33.12.1052-b
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

BMJ

Related search

A Cystic Fibrosis Patient Homozygous for the Nonsense Mutation R553X.

Journal of Medical Genetics
Genetics
1991English

Cystic Fibrosis in a Puerto Rican Female Homozygous for the R1066C Mutation.

Journal of Medical Genetics
Genetics
1998English

Nine Cystic Fibrosis Patients Homozygous for the CFTR Nonsense Mutation R1162X Have Mild or Moderate Lung Disease.

Journal of Medical Genetics
Genetics
1992English

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

Journal of Medical Genetics
Genetics
1993English

GP274 Liver Tests in F508del Homozygous Cystic Fibrosis Patients on Orkambi

2019English

Phenotypic Expression of the p.Leu1077Pro CFTR Mutation in Sicilian Cystic Fibrosis Patients

BMC Research Notes
BiochemistryMedicineGeneticsMolecular Biology
2013English

Preparation for a First-In-Man Lentivirus Trial in Patients With Cystic Fibrosis

Thorax
PulmonaryRespiratory Medicine
2016English

The Cystic Fibrosis F508del Mutation in Crohn's Disease

Journal of Cystic Fibrosis
Child HealthPulmonaryPediatricsPerinatologyRespiratory Medicine
2011English

Genotype-Phenotype Relationship in 12 Patients Carrying Cystic Fibrosis Mutation R334W.

Journal of Medical Genetics
Genetics
1997English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy