Evaluation of copy number variants for genetic hearing loss: a review of current approaches and recent findings.

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Title: Evaluation of copy number variants for genetic hearing loss: a review of current approaches and recent findings.
Authors: Abbasi W; Boston University School of Medicine, Boston, MA, USA.; Boston Children's Hospital, Children's Rare Disease Cohort Initiative, Boston, MA, USA., French CE; Boston Children's Hospital, Children's Rare Disease Cohort Initiative, Boston, MA, USA., Rockowitz S; Boston Children's Hospital, Children's Rare Disease Cohort Initiative, Boston, MA, USA., Kenna MA; Boston Children's Hospital, Children's Rare Disease Cohort Initiative, Boston, MA, USA.; Department of Otolaryngology Head and Neck Surgery, Harvard Medical School, 300 Longwood Ave, BCH 3129, Boston, MA, 02115, USA., Eliot Shearer A; Boston Children's Hospital, Children's Rare Disease Cohort Initiative, Boston, MA, USA. eliot.shearer@childrens.harvard.edu.; Department of Otolaryngology Head and Neck Surgery, Harvard Medical School, 300 Longwood Ave, BCH 3129, Boston, MA, 02115, USA. eliot.shearer@childrens.harvard.edu.
Source: Human genetics [Hum Genet] 2022 Apr; Vol. 141 (3-4), pp. 387-400. Date of Electronic Publication: 2021 Nov 22.
Publication Type: Journal Article; Review
Journal Info: Publisher: Springer Verlag Country of Publication: Germany NLM ID: 7613873 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1432-1203 (Electronic) Linking ISSN: 03406717 NLM ISO Abbreviation: Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:1432-1203
DOI:10.1007/s00439-021-02365-1