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Springer Nature1
Journal
Human Genetics1
Publication Year
20011
Nikki Liburd results 1 · Newest (Page 1/1, per page 25)
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Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndromeNARA Subscribed
Human Genetics · 2001 · Vol. 109 · Issue 5 · Springer
Nikki Liburd; Manju Ghosh; Saima Riazuddin; Sadaf Naz; Shaheen Khan; Zubair Ahmed; Sheikh Riazuddin; Yong Liang; Puthezhath Menon; Tenesha Smith; Ann Smith; Ken-Shiung Chen; James Lupski; Edward Wilcox; Lorraine Potocki; Thomas Friedman
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