𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Prenatal diagnosis of monosomy 1p36: A focus on brain abnormalities and a review of the literature

✍ Scribed by Philippe M. Campeau; Nicholas Ah Mew; Lola Cartier; Katherine L. Mackay; Lisa G. Shaffer; Vazken M. Der Kaloustian; Mary Ann Thomas


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
143 KB
Volume
146A
Category
Article
ISSN
1552-4825

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Prenatal diagnosis of a highly undiffere
✍ Martina DΓΆren; Sevgi Tercanli; Filippo Gullotta; Wolfgang Holzgreve πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 419 KB πŸ‘ 2 views

Intracranial tumours, often presenting with progressive hydrocephalus, are rare congenital diseases accounting for 0.5-1.5 per cent of all cases of brain tumours diagnosed during childhood. The differential diagnosis includes vascular malformations, infarctions, and haemorrhages. Sonographic signs s

Prenatal detection of a 1p36 deletion in
✍ L. Faivre; N. Morichon-Delvallez; G. Viot; J. Martinovic; M. P. Pinson; J. P. Au πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 208 KB πŸ‘ 2 views

The prenatal diagnosis of a 1p36 deletion is reported. The pregnancy was ascertained at 24 weeks of gestation because of the discovery of multiple malformations at ultrasound including hypotelorism, moderate cerebral ventricular dilatation and Ebstein anomaly with secondary cardiac failure. Followin

Prenatal diagnosis of FRA10A: A case rep
✍ Juan De Leon-Luis; Joaquin Santolaya-Forgas; Gregory May; Vijay Tonk; Doug Shelt πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 69 KB πŸ‘ 2 views

## Abstract We report on the prenatal diagnosis of a familial fra10(q23)/del(10)(q23) detected after cellular cultures in non‐folic deprived medium. Β© 2005 Wiley‐Liss, Inc.

Prenatal diagnosis of fetal cerebellar l
✍ Reuven Sharony; Debora Kidron; Rami Aviram; Yoram Beyth; Ron Tepper πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 131 KB πŸ‘ 2 views

The fetal cerebellar structure, size and consistency are looked at in every system survey. Among the acquired cerebellar events that might change the cerebellar consistency are haemorrhage, infections in utero and neoplasia. Additional fetal malformations, if present, assist in making the final diag

Prenatal diagnosis of an 8p23.1 deletion
✍ L. Faivre; N. Morichon-Delvallez; G. Viot; F. Narcy; S. Loison; L. Mandelbrot; M πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 174 KB πŸ‘ 2 views

The prenatal diagnosis of an 8p23.1 deletion is reported. The diagnosis was ascertained at 22 weeks of gestation because of the discovery of a diaphragmatic hernia at ultrasound. Following cytogenetic studies and counselling, the pregnancy was terminated. An autopsy confirmed the presence of a diaph

Prenatal detection of extra structurally
✍ R. J. Hastings; D. L. Nisbet; K. Waters; T. Spencer; L. S. Chitty πŸ“‚ Article πŸ“… 1999 πŸ› John Wiley and Sons 🌐 English βš– 210 KB πŸ‘ 2 views

We present 16 cases, 10 de novo and 6 familial, in which extra structurally abnormal chromosomes (ESACs) were diagnosed prenatally and identified by fluorescence in situ hybridization (FISH) studies with follow up from birth. We review the literature on prenatally diagnosed ESACs arising de novo and