✦ LIBER ✦

ULTRASOUND SCREENING FOR SPINA BIFIDA: CRANIAL AND CEREBELLAR SIGNS

✍ Scribed by Nicolaides, K.H.; Gabbe, S.G.; Campbell, S.; Guidetti, R.

Book ID: 122401939
Publisher: The Lancet
Year: 1986
Tongue: English
Weight: 605 KB
Volume: 328
Category: Article
ISSN: 0140-6736
DOI: 10.1016/S0140-6736(86)91610-7

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Ultrasound screening for spina bifida: C

Ultrasound screening for spina bifida: Cranial and cerebellar signs: K.H. Nicholaides, S. Campbells, S.G. Gabbe, et al. Lancet II:72–74, (July), 1986

✍ Prem Puri 📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 238 KB

Ultrasound screening for fetal spina bif

Ultrasound screening for fetal spina bifida: Bernard et al

✍ Macones, George A.; Stamilio, David M.; Odibo, Anthony; Cahill, Alison 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 213 KB

Small fetal transverse cerebellar diamet

Small fetal transverse cerebellar diameter: a screening test for spina bifida

✍ R. H. B. de Courcy-Wheeler; M. M. Pomeranz; N. J. Wald; 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 English ⚖ 185 KB

OC155: False negatives of cranial signs

OC155: False negatives of cranial signs in the prediction of spina bifida

✍ T. Ghi; G. Pilu; P. Falco; A. Perolo; B. Valeri; D. Santini; M. Segata; N. Rizzo 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 40 KB

Discussion: ‘Ultrasound screening for fe

Discussion: ‘Ultrasound screening for fetal spina bifida,’ by Bernard et al

✍ Macones, George A.; Stamilio, David M.; Odibo, Anthony; Cahill, Alison 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 171 KB

Screening for novel PAX3 polymorphisms a

Screening for novel PAX3 polymorphisms and risks of spina bifida

✍ Wei Lu; Huiping Zhu; Shu Wen; Cecile Laurent; Gary M. Shaw; Edward J. Lammer; Ri 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 135 KB 👁 2 views

## Abstract **BACKGROUND:**__PAX3__ plays an important role in mammalian embryonic development. Known mutations in __PAX3__ are etiologically associated with Waardenburg syndrome and syndromic neural tube defects (NTDs). Mutations in the murine homologue, __pax3__, are responsible for the phenotype