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Publications by Felicity Mehendale

A Syndromic Form of Pierre Robin Sequence Is Caused by 5q23 Deletions Encompassing FBN2 and PHAX

European Journal of Medical Genetics

English

Related publications

Xp11.22 Deletions Encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a Cause of Syndromic X-Linked Intellectual Disability

Multidisciplinary

English

EP13.03: Pierre Robin Sequence Resulting From 1q21.1 Deletion in a Neonate

Ultrasound in Obstetrics and Gynecology

Nuclear Medicine

Ultrasound Technology

Reproductive Medicine

English

G130(P) Airway and Nutritional Management in Pierre Robin Sequence: A Regional Experience

Archives of Disease in Childhood

English

Longitudinal Sleep Outcomes in Neonates With Pierre Robin Sequence Treated Conservatively

Journal of Clinical Sleep Medicine

Respiratory Medicine

English

Understanding the Spectrum of Treatment Options for Infants With Pierre Robin Sequence and Airway Obstruction

Journal of Clinical Sleep Medicine

Respiratory Medicine

English

Diamond-Blackfan Anemia Caused by Chromosome 1p22 Deletion Encompassing RPL5

Human Genome Variation

Molecular Biology

English

Robin Sequence: A Single Treatment Protocol

Jornal de Pediatria

English

Robin Sequence: A Single Treatment Protocol

Jornal de Pediatria

English

Hereditary Cup-Shaped Ears and the Pierre Robin Syndrome.

Journal of Medical Genetics

English