Works matching DE "GENETICS of ear abnormalities"

Results: 11

Congenital stapes malformation: Rare conductive hearing loss in a patient with Waardenburg syndrome.

Published in:

2016

By:

Melzer, Jonathan M.;
Eliason, Michael;
Conley, George S.

Publication type:

journal article

Surgical Treatment of Polyotia.

Published in:

2015

By:

Eun Young Rha;
Dong Hwi Kim;
Jun Hee Byeon

Publication type:

Case Study

Erythematous soft nodules on both ear helices.

Published in:

International Journal of Dermatology, 2016, v. 55, n. 4, p. 385, doi. 10.1111/ijd.12955

By:

Kong, Tae Seok;
Lee, Young Chae;
Han, Tae Young;
Lee, June Hyunkyung;
Son, Sook‐Ja

Publication type:

Article

MicroRNAs in sensorineural diseases of the ear.

Published in:

Frontiers in Molecular Neuroscience, 2013, v. 6, p. 1, doi. 10.3389/fnmol.2013.00052

By:

Ushakov, Kathy;
Rudnicki, Anya;
Avraham, Karen B.

Publication type:

Article

Genome-wide association scan suggests basis for microtia in Awassi sheep.

Published in:

Animal Genetics, 2016, v. 47, n. 4, p. 504, doi. 10.1111/age.12431

By:

Jawasreh, K.;
Boettcher, P. J.;
Stella, A.

Publication type:

Article

Congenital oval or round window malformations in children: Surgical findings and results in 17 cases.

Published in:

2016

By:

Vincent, Robert;
Wegner, Inge;
Derks, Laura S. M.;
Grolman, Wilko

Publication type:

journal article

Atypical 581-kb 22q11.21 Deletion in a Patient with Oculo-Auriculo-Vertebral Spectrum Phenotype.

Published in:

Cytogenetic & Genome Research, 2016, v. 147, n. 2/3, p. 130, doi. 10.1159/000444228

By:

Colovati, Mileny E.S.;
Bragagnolo, Silvia;
Guilherme, Roberta S.;
Dantas, anelisa G.;
Soares, Maria F.;
Kim, Chong a.;
Perez, ana B.a.;
Melaragno, Maria I.

Publication type:

Article

Bilateral implant-retained auricular prosthesis in a patient with Treacher Collins syndrome: a case report.

Published in:

2014

By:

Karakoca Nemli, Seçil;
Gül, Esma Başak;
Bankoğlu Güngör, Merve

Publication type:

Case Study

CHD7 mutations in patients initially diagnosed with Kallmann syndrome – the clinical overlap with CHARGE syndrome.

Published in:

Clinical Genetics, 2009, v. 75, n. 1, p. 65, doi. 10.1111/j.1399-0004.2008.01107.x

By:

Jongmans, M. C. J.;
van Ravenswaaij-Arts, C. M. A.;
Pitteloud, N.;
Ogata, T.;
Sato, N.;
Claahsen-van der Grinten, H. L.;
van der Donk, K.;
Seminara, S.;
Bergman, J. E. H.;
Brunner, H. G.;
Crowley Jr., W. F.;
Hoefsloot, L. H.

Publication type:

Article

High-Fidelity Tissue Engineering of Patient-Specific Auricles for Reconstruction of Pediatric Microtia and Other Auricular Deformities.

Published in:

PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0056506

By:

Reiffel, Alyssa J.;
Kafka, Concepcion;
Hernandez, Karina A.;
Popa, Samantha;
Perez, Justin L.;
Zhou, Sherry;
Pramanik, Satadru;
Brown, Bryan N.;
Ryu, Won Seuk;
Bonassar, Lawrence J.;
Spector, Jason A.

Publication type:

Article

Symmetrical Chorioretinal Colobomata with Craniovertebral Junction Anomalies in CHARGE Syndrome -- A Case Report with Review of Literature.

Published in:

2014

By:

Natung, Tanie;
Goyal, Amit;
Handique, Akash;
Kapoor, Manish

Publication type:

Case Study