✦ LIBER ✦

CRELD1 and GATA4 gene analysis in patients with nonsyndromic atrioventricular canal defects

✍ Scribed by Anna Sarkozy; Giorgia Esposito; Emanuela Conti; Maria Cristina Digilio; Bruno Marino; Raffaele Calabrò; Antonio Pizzuti; Bruno Dallapiccola

Publisher: John Wiley and Sons
Year: 2005
Tongue: English
Weight: 78 KB
Volume: 139A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.31018

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mutations in GATA4, NKX2.5, CRELD1, and

Mutations in GATA4, NKX2.5, CRELD1, and BMP4 are infrequently found in patients with congenital cardiac septal defects

✍ Maximilian G. Posch; Andreas Perrot; Katharina Schmitt; Sebastian Mittelhaus; Ev 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 82 KB 👁 2 views

mRNA Quantification of T-bet, GATA-3, IF

mRNA Quantification of T-bet, GATA-3, IFN-γ, and IL-4 Shows a Defective Th1 Immune Response in the Peripheral Blood from Rheumatoid Arthritis Patients: Link with Disease Activity

✍ Masanori Kawashima; Pierre Miossec 📂 Article 📅 2005 🏛 Springer 🌐 English ⚖ 87 KB

Molecular genetic analysis of human homo

Molecular genetic analysis of human homologs of Caenorhabditis elegans mab-21-like 1 gene in patients with neural tube defects

✍ Elisa Merello; Patrizia De Marco; Anna Moroni; Alessandro Raso; Maria Grazia Cal 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 209 KB 👁 2 views

## Abstract ## BACKGROUND Neural tube defects (NTDs) are complex embryological malformations, affecting 1 in 1,000 live births. Antisense studies have implicated murine __Mab21__ genes as having an important role in neural tube development. We investigated whether __MAB21L1__/__L2__ genes could be