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Publications by Elijah Behr
Genotype–phenotype Association in Patients With SCN4A Mutation – Authors' Reply
The Lancet
Medicine
National Registry for Sudden Unexpected Deaths of Infants and Children in England: Why Do We Need One and Do Families Want One?
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Related publications
Letter: Predicting Azathioprine-Associated Pancreatitis in IBD-phenotype or Genotype? Authors' Reply
Alimentary Pharmacology and Therapeutics
Hepatology
Pharmacology
Gastroenterology
Genotype and Phenotype in Patients With Noonan Syndrome and a RIT1 Mutation
Genetics in Medicine
Medicine
Genetics
Genotype-Phenotype Relationship in 12 Patients Carrying Cystic Fibrosis Mutation R334W.
Journal of Medical Genetics
Genetics
Mutation Analysis of CACNA1S and SCN4A in Patients With Hypokalemic Periodic Paralysis
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Mutation Characterization and Genotype-Phenotype Correlation in Barth Syndrome
American Journal of Human Genetics
Genetics
Prednisolone Response in Patients With COPD * Authors' Reply
Thorax
Pulmonary
Respiratory Medicine
Classification of CFTR Mutation Classes – Authors' Reply
Lancet Respiratory Medicine,The
Pulmonary
Respiratory Medicine
Genotype–phenotype Correlation in BRCA1/2 Mutation-Associated Pancreatic Cancer
British Journal of Cancer
Cancer Research
Oncology
Heterozygous Glucokinase Splicing Mutation - Identical Genotype With Variable Phenotype in a Single Family
Endocrine Abstracts
