✦ LIBER ✦

P19.06: Meckel Gruber syndrome: prenatal diagnosis and autopsy findings

✍ Scribed by H. Akgun; M. T. Ozgun; M. S. Kutuk; S. Uludag; F. Ozturk; T. Okten; M. Basbug

Book ID: 115563409
Publisher: John Wiley and Sons
Year: 2012
Tongue: English
Weight: 45 KB
Volume: 40
Category: Article
ISSN: 0960-7692
DOI: 10.1002/uog.12023

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

P02.71: Prenatal diagnosis of Meckel-Gru

P02.71: Prenatal diagnosis of Meckel-Gruber syndrome

✍ M. Rasidaki; M. Papadaki; S. Mitas; N. Paikopoulos; J. Stratakis; G. Kouvidis 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 38 KB

P16.10: First trimester prenatal diagnos

P16.10: First trimester prenatal diagnosis of the Meckel—Gruber syndrome—case presentation

✍ T. Roszkowski; A. Kucinska-Chahwan; J. Garwolinski; M. Szyszka; G. Jakiel 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 51 KB

Norman–Roberts syndrome: prenatal diagno

Norman–Roberts syndrome: prenatal diagnosis and autopsy findings

✍ Consolato Sergi; Saida Zoubaa; Monika Schiesser 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 242 KB 👁 1 views

P02.72: Prenatal diagnosis of Meckel–Gru

P02.72: Prenatal diagnosis of Meckel–Gruber syndrome in a pregnancy deriving from ICSI

✍ C. Celentano; F. Prefumo; K. Melchiorre; I. D'Emilio; M. Liberati; G. Gallo; Q. 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 38 KB

Prenatal diagnosis of the Meckel syndrom

Prenatal diagnosis of the Meckel syndrome

✍ N. C. Nevin; W. Thompson; G. Davison; W. T. Horner 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 339 KB

Acrofacial dysostosis syndrome type Rodr

Acrofacial dysostosis syndrome type Rodriguez: Prenatal diagnosis and autopsy findings

✍ David Sermer; Nada Quercia; Karen Chong; David Chitayat 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 158 KB 👁 1 views

## Abstract A new lethal form of acrofacial dysostosis (AFD) syndrome was delineated by Rodriguez et al. [Rodriguez et al. (1990); Am J Med Genet 35:484–489]. We report on a male fetus with mandibulofacial dysostosis, including phocomelia‐like upper limb deficiencies and lower limb anomalies which