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)

Cite this

A microdeletion 22q11.2 can resemble Shprintzen-Goldberg omphalocele syndrome [7]. / Strenge, Sibylle; Kujat, Annegret; Zelante, Leopoldo; Froster, Ursula G.

In: American Journal of Medical Genetics, Part A, Vol. 140, No. 24, 15.12.2006, p. 2838-2839.

Research output: Contribution to journalArticle

Strenge, Sibylle ; Kujat, Annegret ; Zelante, Leopoldo ; Froster, Ursula G. / A microdeletion 22q11.2 can resemble Shprintzen-Goldberg omphalocele syndrome [7]. In: American Journal of Medical Genetics, Part A. 2006 ; Vol. 140, No. 24. pp. 2838-2839.
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