The Enamel Phenotype in Homozygous Fam83h Truncation Mice

Molecular genetics & genomic medicine - United States
doi 10.1002/mgg3.724
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Wiley

Related search

Loop-Tail Phenotype in Heterozygous Mice and Neural Tube Defects in Homozygous Mice Result From a Nonsense Mutation in the Vangl2 Gene

Genetics and Molecular Research
MedicineGeneticsMolecular Biology
2013English

213 Initial Explorations Into Genotype-Phenotype Correlations in Psoriasis: The Homozygous Recessive Model

Journal of Investigative Dermatology
BiochemistryDermatologyCell BiologyMolecular Biology
2017English

Phenotype in Homozygous and Heterozygous Carriers of BEST1 Mutations in Autosomal Recessive Bestrophinopathy

Acta Ophthalmologica
MedicineOphthalmology
2018English

Metabolism of Phenylalanine in Mice Homozygous for the Gene ‘Dilute Lethal’

Biochemical Journal
1970English

Ultrastructural Defects in Developing Enamel of Diabetic Mice

Microscopy and Microanalysis
Instrumentation
2002English

4H Leukodystrophy Caused by a Homozygous POLR3B Mutation: Further Delineation of the Phenotype

American Journal of Medical Genetics, Part A
Genetics
2020English

Phenotype Diversity Among Patients With Homozygous Familial Hypercholesterolemia: A Cohort Study

Atherosclerosis
Cardiovascular MedicineCardiology
2016English

Heregulin Ameliorates the Dystrophic Phenotype in MDX Mice

Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
2004English

Evolutionary Analysis of FAM83H in Vertebrates

PLoS ONE
Multidisciplinary
2017English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy