Literature DB >> 17103454

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

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

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Year:  2006        PMID： 17103454     DOI： 10.1002/ajmg.a.31534

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  1 in total

1.  Expanding the fetal phenotype: Prenatal sonographic findings and perinatal outcomes in a cohort of patients with a confirmed 22q11.2 deletion syndrome.

Authors:  Erica Schindewolf; Nahla Khalek; Mark P Johnson; Juliana Gebb; Beverly Coleman; Terrence Blaine Crowley; Elaine H Zackai; Donna M McDonald-McGinn; Julie S Moldenhauer
Journal:  Am J Med Genet A       Date:  2018-07-28       Impact factor: 2.802
  1 in total

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