Search Results

Whole-exome sequencing for screening noise-induced hearing loss susceptibility genes.

• Authors : Fan, Boya (AUTHOR); Wang, Gang (AUTHOR); Liu, Gang (AUTHOR)

Subjects: SEQUENCE analysis; STAINS & staining (Microscopy); COCHLEA

• Source: Acta Oto-Laryngologica. May2023, Vol. 143 Issue 5, p408-415. 8p.

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Education Full Text (H.W. Wilson)

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A nationwide epidemiologic, clinical, genetic study of Usher syndrome in Japan.

• Authors : Yoshimura, Hidekane (AUTHOR); Nishio, Shin-ya (AUTHOR); Isaka, Yuichi (AUTHOR)

Subjects: HOSPITALS; SOCIAL support; DEAFNESSJAPAN

• Source: Acta Oto-Laryngologica. Sep 2021, Vol. 141 Issue 9, p841-846. 6p.

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Explaining Alport syndrome—lessons from the adult nephrology clinic.

• Authors : Mabillard, Holly; Ryan, Rebecca; Tzoumas, Nik

Subjects: ALPORT syndrome; KIDNEY diseases; KIDNEY failure

• Source: Journal of Rare Diseases; 5/13/2024, Vol. 3 Issue 1, p1-26, 26p

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Hereditarian Ideas and Eugenic Ideals at the National Deaf-Mute College

• Authors : Ennis, William Thomas, III

Subjects: Higher Education; Heredity; DeafnessDistrict of Columbia

• Source: ProQuest LLC. 2015Ph.D. Dissertation, The University of Iowa.194

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trend watch.

• Authors : Tweed, Vera

Subjects: DEAFNESS prevention; TYPE 2 diabetes prevention; OSTEOARTHRITIS

• Source: Better Nutrition. Feb2015, Vol. 77 Issue 2, p13-18. 5p. 9 Color Photographs.

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Mosaic trisomy 20 and mitigation in capital crimes sentencing: A review and case report.

• Authors : Montplaisir, Rose (AUTHOR); Lee, Erica (AUTHOR); Moreno‐De‐Luca, Daniel (AUTHOR)

Subjects: TRISOMY; HOMICIDE; PHENOTYPES

• Source: Behavioral Sciences & the Law. Sep2019, Vol. 37 Issue 5, p512-521. 10p. 1 Chart.

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Mutation spectrum and hotspots of the common deafness genes in 314 patients with nonsyndromic hearing loss in Heze area, China.

• Authors : Zhang, Meng (AUTHOR); Han, Yuechen (AUTHOR); Zhang, Fengguo (AUTHOR)

Subjects: GENETICS of deafness; GENES; GENETIC disordersCHINA

• Source: Acta Oto-Laryngologica. Jul2019, Vol. 139 Issue 7, p612-617. 6p.

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The clinical and genetic characteristics of maternally inherited diabetes and deafness (MIDD) with mitochondrial m.3243A > G mutation: A 10‐year follow‐up observation study and literature review.

• Authors : Zheng, Shasha; Wang, Juanjuan; Sun, Minxian

Subjects: LITERATURE reviews; DEAFNESS; MITOCHONDRIAL DNA

• Source: Clinical Case Reports; Feb2024, Vol. 12 Issue 2, p1-9, 9p

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The Inheritance of Hearing Loss and Deafness: A Historical Perspective.

• Authors : Martini, Alessandro; Cozza, Andrea; Di Pasquale Fiasca, Valerio Maria

Subjects: HEARING disorders; DEAFNESS; HEREDITYMENDEL, Gregor, 1822-1884

• Source: Audiology Research; Feb2024, Vol. 14 Issue 1, p116-128, 13p

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