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Publications by Antonio Percesepe
A Syndromic Form of Pierre Robin Sequence Is Caused by 5q23 Deletions Encompassing FBN2 and PHAX
European Journal of Medical Genetics
Medicine
Genetics
Unravelling the Complexity of Inherited Retinal Dystrophies Molecular Testing: Added Value of Targeted Next-Generation Sequencing
BioMed Research International
Immunology
Molecular Biology
Biochemistry
Microbiology
Medicine
Genetics
Related publications
Xp11.22 Deletions Encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a Cause of Syndromic X-Linked Intellectual Disability
PLoS ONE
Multidisciplinary
EP13.03: Pierre Robin Sequence Resulting From 1q21.1 Deletion in a Neonate
Ultrasound in Obstetrics and Gynecology
Nuclear Medicine
Radiology
Ultrasound Technology
Gynecology
Reproductive Medicine
Radiological
Imaging
Obstetrics
Medicine
G130(P) Airway and Nutritional Management in Pierre Robin Sequence: A Regional Experience
Archives of Disease in Childhood
Child Health
Pediatrics
Perinatology
Longitudinal Sleep Outcomes in Neonates With Pierre Robin Sequence Treated Conservatively
Journal of Clinical Sleep Medicine
Pulmonary
Neurology
Respiratory Medicine
Understanding the Spectrum of Treatment Options for Infants With Pierre Robin Sequence and Airway Obstruction
Journal of Clinical Sleep Medicine
Pulmonary
Neurology
Respiratory Medicine
Diamond-Blackfan Anemia Caused by Chromosome 1p22 Deletion Encompassing RPL5
Human Genome Variation
Biochemistry
Genetics
Molecular Biology
Robin Sequence: A Single Treatment Protocol
Jornal de Pediatria
Child Health
Pediatrics
Perinatology
Robin Sequence: A Single Treatment Protocol
Jornal de Pediatria
Child Health
Pediatrics
Perinatology
Hereditary Cup-Shaped Ears and the Pierre Robin Syndrome.
Journal of Medical Genetics
Genetics
