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Frecuencia de la mutación p.Q829X del gen otoferlina (OTOF) en población colombiana con sordera no sindrómica.

• Authors : Ortiz, Lisbeth Morales; Moyano, Nancy Gelvez; Urrego, Luisa Fernanda

• Source: Universitas Médica; abr-jun2012, Vol. 53 Issue 2, p144-153, 10p

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Empowering deaf and hard hearing females toward premarital counseling and genetic screening: An educational intervention based on empowerment model.

• Authors : Zaien, Sahar Z.; El Sayed, Hanan A.; Ibrahim, Heba A.

Subjects: EDUCATION of people with disabilities; MARRIAGE; DEAFNESSSAUDI Arabia

• Source: African Journal of Reproductive Health; 2021 Special Issue, Vol. 25 Issue 1S, p36-49, 14p

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Advances in genetic diagnostics for hereditary hearing loss.

• Authors : Idan, Natali; Brownstein, Zippora; Shivatzki, Shaked

Subjects: DIAGNOSIS of deafness; ATTITUDE (Psychology); MEDICAL genetics

• Source: Journal of Basic & Clinical Physiology & Pharmacology; Sep2013, Vol. 24 Issue 3, p165-170, 6p

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Israel Society for Auditory Research (ISAR): 2013 Annual Scientific Conference.

• Authors : Avraham, Karen B.

Subjects: CONFERENCES & conventions; DEAFNESS; NEUROBIOLOGYISRAEL

• Source: Journal of Basic & Clinical Physiology & Pharmacology; Sep2013, Vol. 24 Issue 3, p163-164, 2p

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Two novel CHD7 variants in patients with typical and mild features of CHARGE syndrome co-occurring with esophageal atresia.

• Authors : Evanovich, Devon Michael; O'Donnell-Luria, Anne; Zendejas, Benjamin

Subjects: ESOPHAGEAL atresia; TRACHEAL fistula; GENETIC counseling

• Source: Journal of Pediatric Surgery Case Reports; Dec2022, Vol. 87, pN.PAG-N.PAG, 1p

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