Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Alexandra Estevinho

Cutis Aplasia as a Clinical Hallmark for the Syndrome Associated With 19q13.11 Deletion: The Possible Role for UBA2 Gene

Molecular Cytogenetics

Molecular Medicine

Molecular Biology

English

Related publications

Aplasia Cutis Congenita of the Scalp

English

Aplasia Cutis Congenita

Journal of Oncology Medicine & Practice

English

Recognizable Neonatal Clinical Features of Aplasia Cutis Congenita

Italian Journal of Pediatrics

English

Aplasia Cutis Congenita: A Simple and Safe Management

Journal of King Abdulaziz University - Medical Sciences

English

Sclerocornea Associated With the Chromosome 22q11.2 Deletion Syndrome

American Journal of Medical Genetics, Part A

English

Usher Syndrome Type 1 Associated With Primary Ciliary Aplasia

Archives of Ophthalmology

English

Aplasia Cutis Congenita of Eyelid: Case Report

Sensory Systems

English

Acidosis: A Possible Trigger for Brugada Syndrome Associated Arrhythmia

Biophysical Journal

English

Supravalvular Aortic Stenosis Associated With a Deletion Disrupting the Elastin Gene.

Journal of Clinical Investigation

English