Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request
Editorial & Opinion

[Genetic screening for deafness].

Subjects: Genetic Testing* ; Neonatal Screening*; Deafness/Deafness/Deafness/*genetics

  • Source: HNO [HNO] 1999 May; Vol. 47 (5), pp. 456.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 2985099R Publication Model: Print Cited Medium: Print

Record details

×
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:

Record details

×
Academic Journal

Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss.

  • Authors : Sloan-Heggen CM; Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology-Head and Neck Surgery, University of Iowa Carver College of Medicine, 200 Hawkins Drive, Iowa City, IA, 52242, USA.; Department of Molecular Physiology and Biophysics, University of Iowa Carver College of Medicine, Iowa City, 52242, IA, USA.

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

  • Source: Human genetics [Hum Genet] 2016 Apr; Vol. 135 (4), pp. 441-450. Date of Electronic Publication: 2016 Mar 11.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium:

Record details

×
Academic Journal

[Hereditary hearing loss: Part 1: diagnostic overview and practical advice].

  • Authors : Burke WF; Klinik für Hals-Nasen-Ohren-Heilkunde, Medizinische Hochschule Hannover, Carl-Neuberg-Str. 1, 30625, Hannover, Deutschland. ; Lenarz T

Subjects: Genetic Counseling/Genetic Counseling/Genetic Counseling/*methods ; Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*methods

  • Source: HNO [HNO] 2013 Apr; Vol. 61 (4), pp. 353-63.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 2985099R Publication Model: Print Cited Medium:

Record details

×
Academic Journal

[Congenital hearing loss. Molecular genetic diagnosis of connexin genes and genetic counselling].

Subjects: Connexins/Connexins/Connexins/*genetics ; Genetic Counseling/Genetic Counseling/Genetic Counseling/*methods ; Genetic Testing/Genetic Testing/Genetic Testing/*methods

  • Source: HNO [HNO] 2005 Sep; Vol. 53 (9), pp. 773-8.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 2985099R Publication Model: Print Cited Medium: Print

Record details

×
Academic Journal

[Mitochondrial A1555G mutation. Molecular genetic diagnosis in sporadic cases of non-syndromic hearing impairment].

Subjects: Polymorphism, Genetic*; Genetic Predisposition to Disease/Genetic Predisposition to Disease/Genetic Predisposition to Disease/*epidemiology ; Genetic Testing/Genetic Testing/Genetic Testing/*methods

  • Source: HNO [HNO] 2004 Nov; Vol. 52 (11), pp. 968-72.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 2985099R Publication Model: Print Cited Medium: Print

Record details

×
Academic Journal

Search for a time- and cost-saving genetic testing strategy for maturity-onset diabetes of the young.

  • Authors : Dusatkova P; Department of Paediatrics, 2nd Faculty of Medicine, Charles University and University Hospital Motol, V Uvalu 84, 15006, Prague, Czech Republic. .; Pavlikova M

Subjects: Diabetes Mellitus, Type 2*/Diabetes Mellitus, Type 2*/Diabetes Mellitus, Type 2*/diagnosis ; Diabetes Mellitus, Type 2*/Diabetes Mellitus, Type 2*/Diabetes Mellitus, Type 2*/genetics ; Genetic Testing*/Genetic Testing*/Genetic Testing*/methodsMason-Type Diabetes

  • Source: Acta diabetologica [Acta Diabetol] 2022 Sep; Vol. 59 (9), pp. 1169-1178. Date of Electronic Publication: 2022 Jun 23.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 9200299 Publication Model: Print-Electronic Cited Medium:

Record details

×
Academic Journal

The PMEL gene and merle (dapple) in the dachshund: cryptic, hidden, and mosaic variants demonstrate the need for genetic testing prior to breeding.

  • Authors : Ballif BC; Paw Print Genetics, Genetic Veterinary Sciences, Inc., 220 E Rowan, Suite 220, Spokane, WA, 99207, USA. .; Emerson LJ

Subjects: Animal Fur/Animal Fur/Animal Fur/*anatomy & histology ; Dogs/Dogs/Dogs/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*veterinary

  • Source: Human genetics [Hum Genet] 2021 Nov; Vol. 140 (11), pp. 1581-1591. Date of Electronic Publication: 2021 Aug 09.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium:

Record details

×
Academic Journal

Improved genetic testing for monogenic diabetes using targeted next-generation sequencing.

  • Authors : Ellard S; Institute for Biomedical and Clinical Science, University of Exeter Medical School, Barrack Road, Exeter EX2 5DW, UK. ; Lango Allen H

Subjects: Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/*diagnosis ; Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/Diabetes Mellitus, Type 2/*genetics ; Genetic Testing/Genetic Testing/Genetic Testing/*methods

  • Source: Diabetologia [Diabetologia] 2013 Sep; Vol. 56 (9), pp. 1958-63. Date of Electronic Publication: 2013 Jun 15.Publisher: Springer Verlag Country of Publication: Germany NLM ID: 0006777 Publication Model: Print-Electronic Cited Medium:

Record details

×
  • 1-9 of  9 results for ""Deafness""