A child with features of Goldenhar syndrome and a novel 1.12 Mb deletion in 22q11.2 by cytogenetics and oligonucleotide array CGH: Is this a candidate region for the syndrome?

J. Xu, Yao-Shan Fan, V. M. Siu

Research output: Contribution to journalArticle

38 Citations (Scopus)
Original languageEnglish
Pages (from-to)1886-1889
Number of pages4
JournalAmerican Journal of Medical Genetics, Part A
Volume146
Issue number14
DOIs
StatePublished - Jul 15 2008

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Goldenhar Syndrome
Chromosome Banding
Chromosomes, Human, Pair 22
Sequence Deletion
Oligonucleotide Array Sequence Analysis
Cytogenetics
Newborn Infant
Phenotype
Pregnancy

ASJC Scopus subject areas

  • Genetics(clinical)

Cite this

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