A microdeletion 22q11.2 can resemble Shprintzen-Goldberg omphalocele syndrome [7]

Sibylle Strenge, Annegret Kujat, Leopoldo Zelante, Ursula G. Froster

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)2838-2839
Number of pages2
JournalAmerican Journal of Medical Genetics, Part A
Volume140
Issue number24
DOIs
Publication statusPublished - Dec 15 2006

ASJC Scopus subject areas

  • Genetics(clinical)

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