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Dll3 and Notch1 genetic interactions model axial segmental and craniofacial malformations of human birth defects.
Loomes, Kathleen M; Stevens, Stacey A; O'Brien, Megan L; Gonzalez, Dorian M; Ryan, Matthew J; Segalov, Michelle; Dormans, Nicholas J; Mimoto, Mizuho S; Gibson, Joshua D; Sewell, William; Schaffer, Alyssa A; Nah, Hyun-Duck; Rappaport, Eric F; Pratt, Stephen C; Dunwoodie, Sally L; Kusumi, Kenro.
Affiliation
  • Loomes KM; Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.
Dev Dyn ; 236(10): 2943-51, 2007 Oct.
Article in En | MEDLINE | ID: mdl-17849441
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Collection: 01-internacional Database: MEDLINE Main subject: Scoliosis / Congenital Abnormalities / Craniofacial Abnormalities / Intracellular Signaling Peptides and Proteins / Receptor, Notch1 / Membrane Proteins Limits: Animals / Humans Language: En Journal: Dev Dyn Journal subject: ANATOMIA Year: 2007 Document type: Article Affiliation country: United States Country of publication: United States
Search on Google
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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Scoliosis / Congenital Abnormalities / Craniofacial Abnormalities / Intracellular Signaling Peptides and Proteins / Receptor, Notch1 / Membrane Proteins Limits: Animals / Humans Language: En Journal: Dev Dyn Journal subject: ANATOMIA Year: 2007 Document type: Article Affiliation country: United States Country of publication: United States