✦ LIBER ✦

Multiple congenital defects associated with maternal use of topical tretinoin

✍ Scribed by AnthonyH. Lipson; Felicity Collins; WilliamS. Webster

Book ID: 119065817
Publisher: The Lancet
Year: 1993
Tongue: English
Weight: 302 KB
Volume: 341
Category: Article
ISSN: 0140-6736
DOI: 10.1016/0140-6736(93)90868-h

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Multiple congenital anomalies associated

Multiple congenital anomalies associated with apparently normal maternal intake of vitamin A: A phenocopy of the isotretinoin syndrome?

✍ Lungarotti, M. S. ;Marinelli, D. ;Mariani, T. ;Calabro, A. ;Opitz, John M. ;Reyn 📂 Article 📅 1987 🏛 John Wiley and Sons 🌐 English ⚖ 498 KB 👁 2 views

Hereditary thrombocythemia caused by a t

Hereditary thrombocythemia caused by a thrombopoietin (THPO) gain-of-function mutation associated with multiple myeloma and congenital limb defects

✍ Stockklausner, Clemens; Echner, Nicole; Klotter, Anne-Christine; Hegenbart, Ute; 📂 Article 📅 2012 🏛 Springer 🌐 English ⚖ 292 KB

Maternal Use of Antiepileptic Drugs and

Maternal Use of Antiepileptic Drugs and the Risk of Major Congenital Malformations: A Joint European Prospective Study of Human Teratogenesis Associated with Maternal Epilepsy

✍ E. B. Samrén; C. M. van Duijn; S. Koch; V. K. Hiilesmaa; H. Klepel; A. H. Bardy; 📂 Article 📅 1997 🏛 Wiley (Blackwell Publishing) 🌐 English ⚖ 968 KB

Association of reduced folate carrier ge

Association of reduced folate carrier gene polymorphism and maternal folic acid use with neural tube defects

✍ Lijun Pei; Jianmeng Liu; Yewu Zhang; Huiping Zhu; Aiguo Ren 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 95 KB 👁 3 views

A maternal dietary pattern characterised

A maternal dietary pattern characterised by fish and seafood in association with the risk of congenital heart defects in the offspring

✍ SA Obermann-Borst; M Vujkovic; JH de Vries; MF Wildhagen; CW Looman; R de Jonge; 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 155 KB

Interstitial deletion of chromosome 2q32

Interstitial deletion of chromosome 2q32-34 associated with multiple congenital anomalies and a urea cycle defect (CPS I deficiency)

✍ Loscalzo, M.L. ;Galczynski, R.L. ;Hamosh, A. ;Summar, M. ;Chinsky, J.M. ;Thomas, 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 164 KB 👁 2 views