Gray Platelet Syndrome: Novel Mutations of the NBEAL2 Gene

American Journal of Hematology - United States
doi 10.1002/ajh.24610
Full Text
Abstract

Available in full text

Categories
Hematology
Date
Authors
Publisher

Wiley

Related search

Identification of Novel ROR2 Gene Mutations in Indian Children With Robinow Syndrome

JCRPE Journal of Clinical Research in Pediatric Endocrinology
Child HealthEndocrinologyPerinatologyPediatricsMetabolismDiabetes
2014English

Novel Mutations in the IRF6 Gene in Brazilian Families With Van Der Woude Syndrome

International Journal of Molecular Medicine
MedicineGenetics
1998English

Usher Syndrome Type III: Revised Genomic Structure of the USH3 Gene and Identification of Novel Mutations

American Journal of Human Genetics
Genetics
2002English

Four Novel Thymidine Phosphorylase Gene Mutations in Mitochondrial Neurogastrointestinal Encephalomyopathy Syndrome (MNGIE) Patients

European Journal of Human Genetics
Genetics
2003English

Mutations in the Nijmegen Breakage Syndrome Gene in Medulloblastomas

Clinical Cancer Research
Cancer ResearchOncology
2008English

Novel CUL7 Biallelic Mutations Alter the Skeletal Phenotype of 3M Syndrome

Human Genome Variation
BiochemistryGeneticsMolecular Biology
2020English

Novel GRN Mutations in Patients With Corticobasal Syndrome

Scientific Reports
Multidisciplinary
2016English

Mutations in the Human TBX4 Gene Cause Small Patella Syndrome

American Journal of Human Genetics
Genetics
2004English

Three Novel Mutations of the PAX6 Gene in Japanese Aniridia Patients

Journal of Human Genetics
Genetics
2007English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy