Concepedia

Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome

Nikki Liburd, Manju Ghosh, Saima Riazuddin, Sadaf Naz, Shaheen Khan, Zubair M. Ahmed, Sheikh Riazuddin, Yong Liang, P.S.N. Menon, Tenesha N. Smith,

Human Genetics · 2001 · 148 citations · 22 references

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References

22

Easy calculations of lod scores and genetic risks on small computers.

G.M. Lathrop, J.-M. Lalouel · PubMed · 1984 · 1.5K citations

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The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells

Karen B. Avraham, Tama Hasson, Karen P. Steel et al. · Nature Genetics · 1995 · 511 citations

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Correction of Deafness in <i>shaker-2</i> Mice by an Unconventional Myosin in a BAC Transgene

Frank J. Probst, Robert A. Fridell, Yehoash Raphael et al. · Science · 1998 · 421 citations

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Interstitial deletion of (17)(p11.2p11.2) in nine patients

Ann C. M. Smith, Loris McGavran, Jeannie Robinson et al. · American Journal of Medical Genetics · 1986 · 407 citations

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Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome

Ken‐Shiung Chen, Prasad Manian, Thearith Koeuth et al. · Nature Genetics · 1997 · 384 citations

, , +16