Search Results

Retrospective Analysis of the Outcomes of Genetic Testing in Patients Suspected to Have Hereditary Hearing Loss or Deafness.

• Authors : Bowden, Acacia; Hubbel, Alexandra; Smith, Lindsay

Subjects: GENETICS of deafness; COCHLEAR implants; SEQUENCE analysis

• Source: American Journal of Audiology. Mar2024, Vol. 33 Issue 1, p233-241. 9p.

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Hereditary deafness carrier screening in 9,993 Chinese individuals.

• Authors : Yanqiu Liu; Lei Wang; Lanlai Yuan

Subjects: MEDICAL screening; DEAFNESS; GENETIC testingCHINA

• Source: Frontiers in Genetics; 2024, p1-7, 7p

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Analysis of deafness susceptibility gene of neonates in northern Guangdong, China.

• Authors : Ma, Zhanzhong; Huang, Wenbo; Xu, Jing

Subjects: DEAFNESS; NEWBORN infants; GENETIC variationGUANGDONG Sheng (China)

• Source: Scientific Reports; 1/3/2024, Vol. 13 Issue 1, p1-5, 5p

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Genetic screening of common genetic deafness in 60,391 women of childbearing age and intervention of birth defects.

• Authors : Linyuan Niu; Liqin Liu; Jinjun Tian

Subjects: GENETIC testing; CHILDBEARING age; DEAFNESS

• Source: Archives of Medical Science; Jan2024, Vol. 20 Issue 1, p113-123, 11p

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Education Full Text (H.W. Wilson)

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Case report: Prenatal diagnosis in the fetus of a couple with both thalassemia and deafness genes.

• Authors : Youqiong Li; Liang Liang; Jinping Bai

Subjects: PRENATAL diagnosis; DEAFNESS; FETUS

• Source: Frontiers in Genetics; 2023, p1-5, 5p

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The responsible genes in Japanese deafness patients and clinical application using Invader assay.

• Authors : Usami, Shin-Ichi (AUTHOR); Wagatsuma, Michio (AUTHOR); Fukuoka, Hisakuni (AUTHOR)

Subjects: GENETICS of deafness; DEAFNESS; DEAF people

• Source: Acta Oto-Laryngologica. Apr2008, Vol. 128 Issue 4, p446-454. 9p. 3 Diagrams, 1 Chart.

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GJB2, SLC26A4 and mitochondrial DNA A1555G mutations in prelingual deafness in Northern Chinese subjects.

• Authors : Guo, Yu-Fen (AUTHOR); Liu, Xiao-Wen (AUTHOR); Guan, Jing (AUTHOR)

Subjects: DEAFNESS; GENES; HUMAN chromosome abnormality diagnosisCHINA

• Source: Acta Oto-Laryngologica. Mar2008, Vol. 128 Issue 3, p297-303. 7p. 3 Charts, 2 Graphs.

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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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Deafness Gene Mutations in Newborns in the Foshan Area of South China With Bloodspot-Based Genetic Screening Tests

• Authors : Cao, Shunwang; Sha, Yanhua; Ke, Peifeng

• Source: American Journal of Audiology. June, 2020, Vol. 29 Issue 2, p165, 5 p.

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