E-LIB Suche - Ergebnisse für: Odent, S.

1

Role of chromosomal imbalances in the pathogenesis of DSD: ..:

Mary, L. ; Fradin, M. ; Pasquier, L....
European Journal of Medical Genetics. 66 (2023) 6 - p. 104748 , 2023

Link: https://doi.org/10.1016/..

2

Cost of exome analysis in patients with intellectual disabi..:

Soilly, AL ; Robert-Viard, C ; Besse, C...
BMC Health Services Research. 23 (2023) 1 - p. , 2023

Link: https://doi.org/10.1186/..

3

Architecture génétique de l'insuffisance ovarienne primitiv..:

Heddar, A. ; Ogur, C. ; Braham, I....
Annales d'Endocrinologie. 83 (2022) 5 - p. 316-317 , 2022

Link: https://doi.org/10.1016/..

4

Angioedeme par mutation du facteur XII : caractéristiques d..:

Ahouach, B. ; Hardy, G. ; Boccon-Gibod, I....
La Revue de Médecine Interne. 42 (2021) - p. A327-A328 , 2021

Link: https://doi.org/10.1016/..

5

Long-term outcomes of artificial urinary sphincter in femal..:

Hascoet, J. ; Manunta, A. ; Brochard, C.B....
European Urology Open Science. 19 (2020) - p. e707 , 2020

Link: https://doi.org/10.1016/..

6

Psycho-social impact of predictive genetic testing in hered..:

Bordet, C. ; Brice, S. ; Maupain, C....
Archives of Cardiovascular Diseases Supplements. 12 (2020) 1 - p. 32-33 , 2020

Link: https://doi.org/10.1016/..

7

P891Psycho-social impact of predictive genetic testing in h..:

Bordet, C ; Brice, S ; Maupain, C...
European Heart Journal. 40 (2019) Supplement_1 - p. , 2019

Link: https://doi.org/10.1093/..

8

Genetic spectrum of hypertrophic cardiomyopathy revisited. ..:

Nguyen, K. ; Roche, S. ; Lavoute, C....
Archives of Cardiovascular Diseases Supplements. 11 (2019) 1 - p. 29 , 2019

Link: https://doi.org/10.1016/..

9

Unexpected diagnosis of a SHH nonsense variant causing a va..:

Bruel, A.‐L. ; Thevenon, J. ; Huet, F....
Clinical Genetics. 94 (2018) 1 - p. 182-184 , 2018

Link: https://doi.org/10.1111/..

10

Incidence des troubles neuropsychiatriques chez les patient..:

Maillot, F. ; Douillard, C. ; Feillet, F....
La Revue de Médecine Interne. 38 (2017) - p. A90-A91 , 2017

Link: https://doi.org/10.1016/..

11

Using medical exome sequencing to identify the causes of ne..:

Chérot, E. ; Keren, B. ; Dubourg, C....
Clinical Genetics. 93 (2017) 3 - p. 567-576 , 2017

Link: https://doi.org/10.1111/..

12

Molecular, clinical and neuropsychological study in 31 pati..:

Lehman, N. ; Mazery, A.C. ; Visier, A....
Clinical Genetics. 92 (2017) 3 - p. 298-305 , 2017

Link: https://doi.org/10.1111/..

13

A series of 38 novel germline and somatic mutations ofNIPBL..:

Nizon, M. ; Henry, M. ; Michot, C....
Clinical Genetics. 89 (2016) 5 - p. 584-589 , 2016

Link: https://doi.org/10.1111/..

14

Complex mode of inheritance in holoprosencephaly revealed b..:

Mouden, C. ; Dubourg, C. ; Carré, W....
Clinical Genetics. 89 (2016) 6 - p. 659-668 , 2016

Link: https://doi.org/10.1111/..

15

Processing and characterization of polyethersulfone wet-spu..:

Bouchard, J. ; Cayla, A. ; Odent, S....
Synthetic Metals. 217 (2016) - p. 304-313 , 2016

Link: https://doi.org/10.1016/..