Suchergebnisse - "Lavillaureix, A"

PubPharm (6)

1

Mayer-Rokitansky-Küster-Hauser syndrome patients' interest, expectations and demands concerning uterus transplantation

enthalten in: Journal of gynecology obstetrics and human reproduction | 2023

von Sousa, C. | Carton, I. | Jaillard, S. | +6

2

Cost of exome analysis in patients with intellectual disability : a micro-costing study in a French setting

enthalten in: BMC health services research | 2023

von Soilly, A. | Robert-Viard, C. | Besse, C. | +68

3

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction

enthalten in: bioRxiv.org | 2022

von den Hoed, J. | de Boer, E. | Voisin, N. | +94

4

Using medical exome sequencing to identify the causes of neurodevelopmental disorders : Experience of 2 clinical units and 216 patients

enthalten in: Clinical genetics | 2018

von Chérot, E. | Keren, B. | Dubourg, C. | +27

5

Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly

enthalten in: Clinical genetics | 2017

von Lavillaureix, A. | Heide, S. | Chantot‐Bastaraud, S. | +8

6

Mosaic intragenic deletion of FBN2 and severe congenital contractural arachnodactyly

enthalten in: Clinical genetics | 2017

von Lavillaureix, A. | Heide, S. | Chantot-Bastaraud, S. | +8

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