E-LIB Suche - Ergebnisse für: Sanlaville, D.

1

CHROMATIN ACCESSIBILITY PROFILING TO INCREASE DIAGNOSTIC AC..:

Julia, E. ; Mareschal, S. ; Chebel, A....
Hematological Oncology. 41 (2023) S2 - p. 192-193 , 2023

Link: https://doi.org/10.1002/..

2

À quel âge faut-il envisager la congélation de spermatozoïd..:

Renault, L. ; Labrune, E. ; Giscard D'Estaing, S....
Annales d'Endocrinologie. 83 (2022) 5 - p. 292-293 , 2022

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

3

Deciphering balanced translocations in infertile males by n..:

Yammine, T ; Reynaud, N ; Lejeune, H...
Molecular Human Reproduction. 27 (2021) 6 - p. , 2021

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

4

Syndrome de Klinefelter, rôle du chromosome Y dans l'espéra..:

Teoli, J. ; Bardel, C. ; Fablet, M....
Annales d'Endocrinologie. 81 (2020) 4 - p. 194 , 2020

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

5

Réflexions éthiques sur le dépistage génétique préconceptio..:

Pujol, P. ; Fodil-Chérif, S. ; Mandel, J.L....
Ethics, Medicine and Public Health. 12 (2020) - p. 100439 , 2020

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

6

Detection of rare autosomal trisomies through non‐invasive ..:

Chatron, N. ; Till, M. ; Abel, C....
Ultrasound in Obstetrics & Gynecology. 53 (2019) 1 - p. 129-130 , 2019

Link: https://doi.org/10.1002/..

7

Secondary findings from next generation sequencing: Psychol..:

Houdayer, F. ; Putois, O. ; Babonneau, M.L....
European Journal of Medical Genetics. 62 (2019) 10 - p. 103711 , 2019

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

8

Secondary findings from whole-exome/genome sequencing evalu..:

Delanne, J. ; Nambot, S. ; Chassagne, A....
European Journal of Medical Genetics. 62 (2019) 6 - p. 103529 , 2019

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

9

Les modifications de pratique clinique liées à l'arrivée du..:

Demougeot, L. ; Houdayer, F. ; Pélissier, A....
Archives de Pédiatrie. 25 (2018) 2 - p. 77-83 , 2018

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

10

Valeur pronostique des altérations génomiques des tumeurs h..:

Lasolle, H. ; Elsensohn, M.H. ; Alix, E....
Annales d'Endocrinologie. 79 (2018) 4 - p. 212 , 2018

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

11

MED13L-related intellectual disability: involvement of miss..:

Smol, T. ; Petit, F. ; Piton, A....
neurogenetics. 19 (2018) 2 - p. 93-103 , 2018

Link: https://doi.org/10.1007/..

12

EP08.02: Cerebral imaging features of a new syndromic entit..:

Guibaud, L. ; Putoux, A. ; Cabet, S....
Ultrasound in Obstetrics & Gynecology. 52 (2018) S1 - p. 222-222 , 2018

Link: https://doi.org/10.1002/..

13

Next-generation sequencing allows a diagnostic yield of 23...:

Lesca, G. ; Labalme, A. ; Mignot, C....
European Journal of Paediatric Neurology. 21 (2017) - p. e168-e169 , 2017

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

14

6q22.1 deletion is associated with epilepsy and abnormal mo..:

Schluth-Bolard, C. ; Flamand-Roze, E. ; Masurel, A....
European Journal of Paediatric Neurology. 21 (2017) - p. e52-e53 , 2017

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

15

Molecular cytogenetic characterization of five F8 complex r..:

Jourdy, Y. ; Chatron, N. ; Fretigny, M....
Haemophilia. 23 (2017) 4 - p. , 2017

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