Unstable Mutations in the FMR1 Gene and the Phenotypes

Advances in Experimental Medicine and Biology - United States
doi 10.1007/978-1-4614-5434-2_6
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Springer New York

Related search

Variable Retinal Phenotypes Caused by Mutations in the X-Linked Photopigment Gene Array

Investigative Ophthalmology and Visual Science
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2010English

Heterogeneous Pulmonary Phenotypes Associated With Mutations in the Thyroid Transcription Factor Gene NKX2-1

Chest
CardiologyCritical CareCardiovascular MedicineIntensive Care MedicinePulmonaryRespiratory Medicine
2013English

Sequencing the Unsequenceable: Expanded CGG Repeats in the Human FMR1 Gene

Biophysical Journal
Biophysics
2013English

The FMR1 Gene, Infertility, and Reproductive Decision-Making: A Review

Frontiers in Genetics
GeneticsMolecular Medicine
2014English

Mutations in the LHX3 Gene Cause Dysregulation of Pituitary and Neural Target Genes That Reflect Patient Phenotypes

Gene
MedicineGenetics
2007English

412 Hairless ( Hr ) Mutations and Phenotypes: The New and the Old

Journal of Investigative Dermatology
BiochemistryDermatologyCell BiologyMolecular Biology
2016English

Characterization of ABCC8 and KCNJ11 Gene Mutations and Phenotypes in Korean Patients With Congenital Hyperinsulinism

European Journal of Endocrinology
MedicineEndocrinologyMetabolismDiabetes
2011English

From Lowe Syndrome to Dent Disease: Correlations Between Mutations of the OCRL1 Gene and Clinical and Biochemical Phenotypes

Human Mutation
Genetics
2011English

Disabilities Caused by Unstable Mutations in Costa Rica

Revista de Biologia Tropical
AgriculturalBiological Sciences
2014English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy