Amanote Research
Register
Sign In
Cystic Fibrosis in a Puerto Rican Female Homozygous for the R1066C Mutation.
Journal of Medical Genetics
- United Kingdom
doi 10.1136/jmg.35.1.84-a
Full Text
Open PDF
Abstract
Available in
full text
Categories
Genetics
Date
January 1, 1998
Authors
M H Liang
L J Wong
D Klein
B Shapiro
C M Bowman
E Hsu
L J Wong
Publisher
BMJ
Related search
A Cystic Fibrosis Patient Homozygous for the Nonsense Mutation R553X.
Journal of Medical Genetics
Genetics
Severe Cystic Fibrosis in a Child Homozygous for the G542 Nonsense Mutation in the CFTR Gene.
Journal of Medical Genetics
Genetics
First Report of Three Cystic Fibrosis Patients Homozygous for the 1717-1g-->A Mutation.
Journal of Medical Genetics
Genetics
Nine Cystic Fibrosis Patients Homozygous for the CFTR Nonsense Mutation R1162X Have Mild or Moderate Lung Disease.
Journal of Medical Genetics
Genetics
The Cystic Fibrosis F508del Mutation in Crohn's Disease
Journal of Cystic Fibrosis
Child Health
Pulmonary
Pediatrics
Perinatology
Respiratory Medicine
Conserving the Puerto Rican Herpetofauna
Applied Herpetology
Mutations in COL27A1 Cause Steel Syndrome and Suggest a Founder Mutation Effect in the Puerto Rican Population
European Journal of Human Genetics
Genetics
GP274 Liver Tests in F508del Homozygous Cystic Fibrosis Patients on Orkambi
A G542X Cystic Fibrosis Mouse Model for Examining Nonsense Mutation Directed Therapies
PLoS ONE
Multidisciplinary