![Notch-2 / Notch proteins / Notch signaling pathway / Alagille syndrome / Congenital heart defect / Ankyrin repeat / JAG1 / Mutation / Insertion / Biology / Health / Genetics Notch-2 / Notch proteins / Notch signaling pathway / Alagille syndrome / Congenital heart defect / Ankyrin repeat / JAG1 / Mutation / Insertion / Biology / Health / Genetics](https://www.pdfsearch.io/img/0f4a8863ff2653ecc373253d40bf8ce5.jpg)
| Document Date: 2012-07-05 15:59:41 Open Document File Size: 284,16 KBShare Result on Facebook
City Strasbourg / Dijon / Nantes / NOTCH2 cDNA / Paris / Lausanne / Illkirch / / Company A.D. / GenBank / Agilent / L.F. / V.C.-D. / B.I. / S.B. / C.L.C. / M.W. & Kulozik A.E. / Nature America Inc. / Google / / Country Switzerland / France / / / Facility C terminus / / IndustryTerm Open-source software / ONLINE PUBLICATION / aDVANCE ONLINE PUBLICATION / / MedicalCondition PDA / Hypospadias / Hajdu-Cheney syndrome / hypertelorism / Alagille syndrome / polycystic kidneys / prognathism / Congenital heart defect PDA / T-cell acute lymphoblastic leukemia / N LS PE ST Hajdu-Cheney syndrome / K Hajdu-Cheney syndrome / periodontal disease / Neurologic symptoms / osteopenia / HajduCheney syndrome / congenital heart defects / rare skeletal disorder / Alzheimer’s disease / cancer / disease / Umbilical hernia / acro-osteolysis / patent ductus arteriosus / stroke / Iris coloboma / ventricular septal defect / spondylocostal dysostosis / inguinal hernia / cleft palate / NOTCH2 dysfunction / monogenic disorders / osteoporosis / rare autosomal dominant skeletal disorder / platybasia / syndrome / / Organization L’Institut / Centre de Référence Maladies Rares / Centre Hospitalier / / Person Nat / Enfants Malades / / Position General / AUTHOR / / PublishedMedium Nature Genetics / / RadioStation R AM / / Technology java / gene expression / PDA / / URL http /
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