[Studies on the genetics and pathology of the development of 8 labyrinth mutants (deaf-waltzer-shaker mutants) in the mouse (Mus musculus)].
作者信息
KOCHER W
出版信息
Z Vererbungsl. 1960;91:114-40.
PMID:13853422
Abstract
摘要
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引用本文的文献
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[Research on the genetics and pathology of the development of delayed hereditary deafness in the mouse (Mus musculus)].
Arch Ohren Nasen Kehlkopfheilkd. 1960;177:108-45.
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Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2.
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本文引用的文献
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Histological studies of endolymph secretion and resorption in the inner ear.
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[Congenital malformations of the auditory organs in mice].
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[Morphological and microscopic anatomical studies on the inner ear of a species of spontaneously mutant house mice (turning mice)].
Z Mikrosk Anat Forsch. 1956;62(3):348-406.
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[Studies on the inner ear of a deaf domestic mouse mutant with motor disorders in comparison with hereditary labyrinthine hearing disorders in man].
Arch Ohren Nasen Kehlkopfheilkd. 1957;170(4):411-33.
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[Differentiation processes in the epithelium of ductus cochlearis].
Acta Anat (Basel). 1957;29(1-2):53-90.
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An annotated catalogue of the mutant genes of the house mouse.
Memo Med Res Counc. 1956;43(33):1-28.
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The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse.
Proc R Soc Lond B Biol Sci. 1956 May 29;145(919):206-13. doi: 10.1098/rspb.1956.0028.
9
Hereditary lesions of the labyrinth in the mouse.
Br Med Bull. 1956 May;12(2):153-7. doi: 10.1093/oxfordjournals.bmb.a069538.
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