Format

Send to

Choose Destination
Prenat Diagn. 2019 Apr;39(5):388-393. doi: 10.1002/pd.5439. Epub 2019 Apr 1.

Prenatal diagnosis of fragile X syndrome: Small meiotic recombination events at the FMR1 locus.

Author information

1
Université Paris Descartes - Sorbonne Paris Cite, Institut Imagine UMR1163, Fédération de Génétique médicale, Hôpital universitaire Necker-Enfants Malades, AP-HP, Paris, France.
2
Service de gynécologie obstétrique, Centre hospitalier de Blois, Blois, France.
3
Service de Génétique, CHRU de Tours, UMR 1253, iBrain, Université de Tours, Inserm, Tours, France.

Abstract

in French
PMID:
30779209
DOI:
10.1002/pd.5439

Supplemental Content

Full text links

Icon for Wiley
Loading ...
Support Center