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Notch-2 / Notch proteins / Notch signaling pathway / Alagille syndrome / Congenital heart defect / Ankyrin repeat / JAG1 / Mutation / Insertion / Biology / Health / Genetics


b r i e f c o m m u n i c at i o n s b EGF repeats (n = 36)
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Document Date: 2012-07-05 15:59:41


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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 / /

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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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