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 journal › Article

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

Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss [2]. / Yan, Denise; Xiao, Mei Ouyang; Angeli, Simon I; Li, Lin Du; Liu, Xue Z.

In: American Journal of Medical Genetics, Part A, Vol. 143, No. 4, 15.02.2007, p. 385-386.

Research output: Contribution to journal › Article

Yan, D, Xiao, MO, Angeli, SI, Li, LD & Liu, XZ 2007, 'Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss [2]', American Journal of Medical Genetics, Part A, vol. 143, no. 4, pp. 385-386. https://doi.org/10.1002/ajmg.a.31553
Yan D, Xiao MO, Angeli SI, Li LD, Liu XZ. Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss [2]. American Journal of Medical Genetics, Part A. 2007 Feb 15;143(4):385-386. https://doi.org/10.1002/ajmg.a.31553
Yan, Denise ; Xiao, Mei Ouyang ; Angeli, Simon I ; Li, Lin Du ; Liu, Xue Z. / Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss [2]. In: American Journal of Medical Genetics, Part A. 2007 ; Vol. 143, No. 4. pp. 385-386.
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