NR2F1 deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafness. (Q51937117)
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scientific article published in May 2009
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English | NR2F1 deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafness. |
scientific article published in May 2009 |
Statements
NR2F1 deletion in a patient with a de novo paracentric inversion, inv(5)(q15q33.2), and syndromic deafness. (English)
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Fowzan S Alkuraya
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Kerry K Brown
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Michael Matos
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Virginia E Kimonis
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Cynthia C Morton
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1 May 2009
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149A
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5
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931-938
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Identifiers
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