Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss [2]

Denise Yan, Mei Ouyang Xiao, Simon I Angeli, Lin Du Li, Xue Z Liu

Research output: Contribution to journalArticle

9 Citations (Scopus)
Original languageEnglish
Pages (from-to)385-386
Number of pages2
JournalAmerican Journal of Medical Genetics, Part A
Volume143
Issue number4
DOIs
StatePublished - Feb 15 2007

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Uniparental Disomy
Chromosomes, Human, Pair 13
Connexins
Sequence Deletion
Homozygote
Hearing Loss
Gene Frequency
Mutation
Genes
Uniparental disomy of 13

ASJC Scopus subject areas

  • Genetics(clinical)

Cite this

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title = "Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss [2]",
author = "Denise Yan and Xiao, {Mei Ouyang} and Angeli, {Simon I} and Li, {Lin Du} and Liu, {Xue Z}",
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journal = "American Journal of Medical Genetics, Part C: Seminars in Medical Genetics",
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AU - Li, Lin Du

AU - Liu, Xue Z

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JO - American Journal of Medical Genetics, Part C: Seminars in Medical Genetics

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