Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Neda Stefanović

Hypodontia and WNT10A Mutation: A Case Report

Stomatoloski glasnik Srbije
2018English

Related publications

WNT10A Polymorphism May Be a Risk Factor for Non-Syndromic Hypodontia

Genetics and Molecular Research
MedicineGeneticsMolecular Biology
2016English

Non Syndromic Familial Hypodontia - A Case Series

Stomatology Edu Journal
2018English

Amelogenesis Imperfecta, Hypodontia and Impacted Teeth, a Challenging Case for Rehabilitation

Clinical Oral Implants Research
Oral Surgery
2017English

A Common Founder Mutation in the EDA-A1 Gene in X-Linked Hypodontia

Dermatology
Dermatology
2010English

Cognitive Impairment and Fabry Disease: A Case Report With Mutation S126G

Neuropsychological Trends
Molecular NeurosciencePhysiological PsychologyNeuropsychologyCellular
2016English

Thrombocytosis in an Infant With a TRPV4 Mutation: A Case Report

2020English

BCS1L Gene Mutation Causing GRACILE Syndrome: Case Report

Renal Failure
MedicineNephrologyCritical CareIntensive Care Medicine
2014English

A New Mutation in IDS Gene Causing Hunter Syndrome: A Case Report

Frontiers in Genetics
GeneticsMolecular Medicine
2020English

PALB2 Mutation in a Woman With Bilateral Breast Cancer: A Case Report

Molecular and Clinical Oncology
Cancer ResearchOncology
2017English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy