Familial Syndromic Esophageal Atresia Maps to 2p23-p24

Esophageal atresia (EA) is a common life-threatening congenital anomaly that occurs in 1/3,000 newborns. Little is known of the genetic factors that underlie EA. Oculodigitoesophageoduodenal (ODED) syndrome (also known as “Feingold syndrome”) is a rare autosomal dominant disorder with digital abnorm...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Celli, Jacopo, van Beusekom, Ellen, Hennekam, Raoul C. M., Gallardo, M. Esther, Smeets, Dominique F. C. M., de Córdoba, Santiago Rodríguez, Innis, Jeffrey W., Frydman, Moshe, König, Rainer, Kingston, Helen, Tolmie, John, Govaerts, Lutgarde C. P., van Bokhoven, Hans, Brunner, Han G.
Médium: Artigo
Jazyk:Inglês
Vydáno: The American Society of Human Genetics 2000
Témata:
Articles
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1288096/
https://ncbi.nlm.nih.gov/pubmed/10677303
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky