The mouse deafness locus (dn) is associated with an inversion on chromosome 19

Ana M. Viñas; Stacy S. Drury; Margaret M. Deangelis; Zhining Den; Jer Min Huang; Charles I. Berlin; Jay D. Hunt; Mark A. Batzer; Prescott L. Deininger; Bronya J.b. Keats

doi:10.1016/S0925-4439(98)00050-7

The mouse deafness locus (dn) is associated with an inversion on chromosome 19

Ana M. Viñas
, Stacy S. Drury
, Margaret M. Deangelis
, Zhining Den
, Jer Min Huang
, Charles I. Berlin
, Jay D. Hunt
, Mark A. Batzer
, Prescott L. Deininger
, Bronya J.b. Keats

Department of Ophthalmology

University Medical Center New Orleans
Louisiana Stt. Univ. Med. C.
Louisiana State University Health Sciences Center

Research output: Contribution to journal › Article › peer-review

4 Scopus citations

Abstract

Recombination data for the mouse deafness locus (dn) on chromosome 19 are consistent with the presence of an inversion for which one of the breakpoints is between D19Mit14 and D19Mit96, a distance of less than 226 kb. Fluorescence in situ hybridization studies using a bacterial artificial chromosome on interphase (G₁) nuclei provide additional support for the presence of an inversion. The dn gene is probably the orthologue of the human DFNB7/DFNB11 gene on chromosome 9. Copyright (C) 1998 Elsevier Science B.V.

Original language	English
Pages (from-to)	257-262
Number of pages	6
Journal	Biochimica et Biophysica Acta - Molecular Basis of Disease
Volume	1407
Issue number	3
DOIs	https://doi.org/10.1016/S0925-4439(98)00050-7
State	Published - Sep 30 1998

Keywords

Chromosome 19
Deafness
Inversion
Mouse
Non-syndromic hearing impairment

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10.1016/S0925-4439(98)00050-7

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title = "The mouse deafness locus (dn) is associated with an inversion on chromosome 19",

abstract = "Recombination data for the mouse deafness locus (dn) on chromosome 19 are consistent with the presence of an inversion for which one of the breakpoints is between D19Mit14 and D19Mit96, a distance of less than 226 kb. Fluorescence in situ hybridization studies using a bacterial artificial chromosome on interphase (G1) nuclei provide additional support for the presence of an inversion. The dn gene is probably the orthologue of the human DFNB7/DFNB11 gene on chromosome 9. Copyright (C) 1998 Elsevier Science B.V.",

keywords = "Chromosome 19, Deafness, Inversion, Mouse, Non-syndromic hearing impairment",

author = "Vi{\~n}as, \{Ana M.\} and Drury, \{Stacy S.\} and Deangelis, \{Margaret M.\} and Zhining Den and Huang, \{Jer Min\} and Berlin, \{Charles I.\} and Hunt, \{Jay D.\} and Batzer, \{Mark A.\} and Deininger, \{Prescott L.\} and Keats, \{Bronya J.b.\}",

year = "1998",

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doi = "10.1016/S0925-4439(98)00050-7",

language = "English",

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TY - JOUR

T1 - The mouse deafness locus (dn) is associated with an inversion on chromosome 19

AU - Viñas, Ana M.

AU - Drury, Stacy S.

AU - Deangelis, Margaret M.

AU - Den, Zhining

AU - Huang, Jer Min

AU - Berlin, Charles I.

AU - Hunt, Jay D.

AU - Batzer, Mark A.

AU - Deininger, Prescott L.

AU - Keats, Bronya J.b.

PY - 1998/9/30

Y1 - 1998/9/30

N2 - Recombination data for the mouse deafness locus (dn) on chromosome 19 are consistent with the presence of an inversion for which one of the breakpoints is between D19Mit14 and D19Mit96, a distance of less than 226 kb. Fluorescence in situ hybridization studies using a bacterial artificial chromosome on interphase (G1) nuclei provide additional support for the presence of an inversion. The dn gene is probably the orthologue of the human DFNB7/DFNB11 gene on chromosome 9. Copyright (C) 1998 Elsevier Science B.V.

AB - Recombination data for the mouse deafness locus (dn) on chromosome 19 are consistent with the presence of an inversion for which one of the breakpoints is between D19Mit14 and D19Mit96, a distance of less than 226 kb. Fluorescence in situ hybridization studies using a bacterial artificial chromosome on interphase (G1) nuclei provide additional support for the presence of an inversion. The dn gene is probably the orthologue of the human DFNB7/DFNB11 gene on chromosome 9. Copyright (C) 1998 Elsevier Science B.V.

KW - Chromosome 19

KW - Deafness

KW - Inversion

KW - Mouse

KW - Non-syndromic hearing impairment

UR - https://www.scopus.com/pages/publications/18244413205

U2 - 10.1016/S0925-4439(98)00050-7

DO - 10.1016/S0925-4439(98)00050-7

M3 - Article

C2 - 9748617

AN - SCOPUS:18244413205

SN - 0925-4439

VL - 1407

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JO - Biochimica et Biophysica Acta - Molecular Basis of Disease

JF - Biochimica et Biophysica Acta - Molecular Basis of Disease

IS - 3

ER -

The mouse deafness locus (dn) is associated with an inversion on chromosome 19

Abstract

Keywords

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