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Case report

First published 2023-6

A Clinical Report of the Complete Nasal Agenesis: Reconstruction of Congenital Arhinia and Review of the Literature

Etkin Boynuyogun, Gokhan Tuncbilek

The Cleft Palate Craniofacial Journal

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Case report

First published 2023-4

A Case Report on Lateral Proboscis: A Rare Congenital Anomaly

Indri Lakhsmi Putri, Taufiqur Rakhim Aditra, Tedy Apriawan [...]

The Cleft Palate Craniofacial Journal

Free access

Research article

First published 2008-1

Unilateral Inferior Turbinate Agenesis: A Case Report

Fatma Çaylakli, Ismail Yilmaz, Cem Hürcan [...]

Ear,Nose & Throat Journal

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Research article

First published 1991-1

Five Cases of DeMyer Sequence: An Interophthalmic Dysplasia

John L. Spolyar, Frances Eldis, David Benjamins

The Cleft Palate Craniofacial Journal

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Case report

First published 2021-9

Surgical Management of Velopharyngeal Insufficiency Due to Unilateral Oropharyngeal Agenesis in a Patient With Stickler Syndrome

Bronson Wessinger, Kyle Kimura, James Phillips [...]

The Cleft Palate Craniofacial Journal

Open access

Case report

First published 2023-9

An Endoscopic Endonasal Attempt at Pediatric Meningoencephalocele Repair

Jonathan Raskin, Michela Borrelli, Bozena Wrobel

Ear,Nose & Throat Journal

Free access

Research article

First published 2024-1

Orofacial Deformities in 3 Related Rhesus Monkeys ( Macaca mulatta ) Resembling Human Binder’s Syndrome

Beatriz Goldschmidt, Aline C. Bouzon, Bárbara C. S. Meireles [...]

The Cleft Palate Craniofacial Journal

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Research article

First published 2004-3

Craniofacial Morphology in an Unusual Case with Nasal Aplasia Studied by Roentgencephalometry and Three-Dimensional CT Scanning

Noriyuki Kitai, Yoshitaka Iguchi, Mariko Takashima [...]

The Cleft Palate Craniofacial Journal

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Research article

First published 1996-3

Paranasal Sinus Computed Tomography Scan Findings in Patients with Cystic Fibrosis

Gary J. Nishioka, Paul R. Cook, Joel P. McKinsey [...]

Otolaryngology–Head and Neck Surgery

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Research article

First published 2003-5

Biochemical Abnormality Associated with Smith-Lemli-Opitz Syndrome in an Infant with Features of Rutledge Multiple Congenital Anomaly Syndrome Confirms that the Latter is a Variant of the Former

Dinesh Rakheja, Golder N. Wilson, Beverly B. Rogers

Pediatric and Developmental Pathology

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