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Academic Journal

Exome sequencing in infants with congenital hearing impairment: a population-based cohort study.

Subjects: Genetic Testing/Genetic Testing/Genetic Testing/*standards ; Hearing Loss/Hearing Loss/Hearing Loss/*genetics ; Neonatal Screening/Neonatal Screening/Neonatal Screening/*standards

  • Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2020 May; Vol. 28 (5), pp. 587-596. Date of Electronic Publication: 2019 Dec 12.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Concurrent hearing and genetic screening in a general newborn population.

  • Authors : Guo L; Jining Maternal and Child Health Care Service Center, Jining, 272000, China.; Xiang J

Subjects: Genetic Testing* ; Hearing Loss*/Hearing Loss*/Hearing Loss*/diagnosis ; Hearing Loss*/Hearing Loss*/Hearing Loss*/genetics

  • Source: Human genetics [Hum Genet] 2020 Apr; Vol. 139 (4), pp. 521-530. Date of Electronic Publication: 2020 Jan 30.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Genetic screening as an adjunct to universal newborn hearing screening: literature review and implications for non-congenital pre-lingual hearing loss.

  • Authors : D'Aguillo C; Department of Otolaryngology, University of Miami Miller School of Medicine, Miami, FL, USA.; Bressler S

Subjects: Genetic Testing* ; Hearing Tests* ; Neonatal Screening*

  • Source: International journal of audiology [Int J Audiol] 2019 Dec; Vol. 58 (12), pp. 834-850. Date of Electronic Publication: 2019 Jul 02.Publisher: Informa Healthcare Country of Publication: England NLM ID: 101140017 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Nationwide population genetic screening improves outcomes of newborn screening for hearing loss in China.

  • Authors : Wang Q; Department of Otolaryngology-Head and Neck Surgery, Chinese PLA Institute of Otolaryngology, Chinese PLA General Hospital, Beijing, China.; Xiang J

Subjects: Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hearing Loss/Hearing Loss/Hearing Loss/*genetics ; Neonatal Screening/Neonatal Screening/Neonatal Screening/*methods

  • Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2019 Oct; Vol. 21 (10), pp. 2231-2238. Date of Electronic Publication: 2019 Mar 20.Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Assessment of Hearing Screening Combined With Limited and Expanded Genetic Screening for Newborns in Nantong, China.

  • Authors : Zhu QW; Clinical Medicine Research Center, Nantong Maternal and Child Health Hospital affiliated to Nantong University, Nantong, China.; Li MT

Subjects: Genetic Testing* ; Hearing Tests*; Hearing Loss/Hearing Loss/Hearing Loss/*diagnosis

  • Source: JAMA network open [JAMA Netw Open] 2021 Sep 01; Vol. 4 (9), pp. e2125544. Date of Electronic Publication: 2021 Sep 01.Publisher: American Medical Association Country of Publication: United States NLM ID: 101729235 Publication Model: Electronic Cited Medium: Internet

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Academic Journal

Combined hearing screening and genetic screening of deafness among Hakka newborns in China.

  • Authors : Zeng X; Laboratory of Medical Genetics, Heyuan Women and Children's Hospital, Heyuan, Guangdong, China; Department of Clinical Laboratory, Heyuan Women and Children's Hospital, Heyuan, Guangdong, China. Electronic address: .

Subjects: Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hearing Loss/Hearing Loss/Hearing Loss/*diagnosis ; Hearing Tests/Hearing Tests/Hearing Tests/*methods

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2020 Sep; Vol. 136, pp. 110120. Date of Electronic Publication: 2020 Jun 17.Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

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Academic Journal

Screening for GJB2-R143W-Associated Hearing Impairment: Implications for Health Policy and Practice in Ghana.

  • Authors : Adadey SM; West African Centre for Cell Biology of Infectious Pathogens (WACCBIP), University of Ghana, Accra, Ghana.; Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Subjects: Genetic Testing*; Connexin 26/Connexin 26/Connexin 26/*genetics ; Hearing Loss/Hearing Loss/Hearing Loss/*diagnosis

  • Source: Public health genomics [Public Health Genomics] 2020; Vol. 23 (5-6), pp. 184-189. Date of Electronic Publication: 2020 Dec 10.Publisher: S. Karger Country of Publication: Switzerland NLM ID: 101474167 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

[Study of newborn hearing and genetic screening in Jinan].

  • Authors : Xiang L; Department of Newborn Hearing Screening, Jinan Maternity and Child Care Hospital, Jinnan 250001, China.; Lin Q

Subjects: Genetic Testing* ; Hearing Tests* ; Neonatal Screening*

  • Source: Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery [Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi] 2015 May; Vol. 50 (5), pp. Publisher: Zhonghua yi xue hui za zhi she Country of Publication: China NLM ID: 101247574 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

[The effects of newborn genetic screening for GJB2 and hearing follow-ups].

Subjects: Genetic Testing* ; Mutation* ; Neonatal Screening*

  • Source: Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery [Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi] 2015 Feb; Vol. 29 (4), Publisher: Lin chuang er bi yan hou tou jing wai ke za zhi bain ji bu Country of Publication: China NLM ID: 101303164 Publication Model: Print Cited Medium:

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Academic Journal

Newborn hearing concurrent genetic screening for hearing impairment-a clinical practice in 58,397 neonates in Tianjin, China.

  • Authors : Zhang J; BGI-Tianjin, Tianjin, China; Tianjin Medical Genomics Technology Engineering Center, Tianjin, China.

Subjects: Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*epidemiology ; Genetic Testing/Genetic Testing/Genetic Testing/*methods ; Hearing Loss/Hearing Loss/Hearing Loss/*diagnosis

  • Source: International journal of pediatric otorhinolaryngology [Int J Pediatr Otorhinolaryngol] 2013 Dec; Vol. 77 (12), pp. 1929-35. Date of Electronic Publication: 2013 Sep 08.Publisher: Elsevier Scientific Publishers Country of Publication: Ireland NLM ID: 8003603 Publication Model: Print-Electronic Cited Medium: Internet

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  • 1-10 of  2,252 results for ""Neonatal Screening""