E-LIB Suche - Ergebnisse für: Lucas, Josette

1

Cat eye syndrome: Clinical, cytogenetics and familial findi..:

Jedraszak, Guillaume ; Jobic, Florence ; Receveur, Aline...
American Journal of Medical Genetics Part A. 194 (2023) 4 - p. , 2023

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

2

DPNI et discordance fœto-placentaire : à propos de 6 cas:

Beaumont, Marion ; Lucas, Josette ; Launay, Erika...
Morphologie. 102 (2018) 338 - p. 140 , 2018

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

3

Dépistage prénatal non invasif (DPNI) de la trisomie 21 : b..:

Launay, Erika ; Nouyou, Bénédicte ; Le Bouar, Gwenaelle...
Morphologie. 101 (2017) 335 - p. 261 , 2017

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

4

Amplification d'ATM de type HSR dans un lymphome T de bas g..:

Toujani, Saloua ; Henry, Catherine ; Jacomy, Dominique...
Morphologie. 100 (2016) 330 - p. 180-181 , 2016

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

5

Karyotype is not dead (yet)!:

Pasquier, Laurent ; Fradin, Mélanie ; Chérot, Elouan...
European Journal of Medical Genetics. 59 (2016) 1 - p. 11-15 , 2016

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

6

Inversions autosomiques et troubles de la reproduction:

Beaumont, Marion ; Lucas, Josette ; Akloul, Linda...
Morphologie. 100 (2016) 330 - p. 161-162 , 2016

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

7

Clinical and molecular delineation of Tetrasomy 9p syndrome..:

El Khattabi, Laïla ; Jaillard, Sylvie ; Andrieux, Joris...
American Journal of Medical Genetics Part A. 167 (2015) 6 - p. 1252-1261 , 2015

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

8

Postnatal diagnosis of 9q interstitial imbalances involving..:

Blanchard, Marina ; Dubourg, Christèle ; Pasquier, Laurent...
European Journal of Medical Genetics. 57 (2014) 5 - p. 195-199 , 2014

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

9

Inversion duplication deletions involving the long arm of c..:

Quelin, Chloe ; Spaggiari, Emmanuel ; Khung‐Savatovsky, Suonavy...
American Journal of Medical Genetics Part A. 164 (2014) 10 - p. 2504-2509 , 2014

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

10

5q12.1 deletion: Delineation of a phenotype including menta..:

Jaillard, Sylvie ; Andrieux, Joris ; Plessis, Ghislaine...
American Journal of Medical Genetics Part A. 155 (2011) 4 - p. 725-731 , 2011

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

11

Terminal 6.9 Mb deletion of chromosome 15q, associated with..:

Jaillard, Sylvie ; Loget, Philippe ; Lucas, Josette...
European Journal of Medical Genetics. 54 (2011) 2 - p. 186-188 , 2011

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

12

New insights into the pathogenesis of beckwith-wiedemann an..:

Demars, Julie ; Rossignol, Sylvie ; Netchine, Irène...
Human Mutation. 32 (2011) 10 - p. 1171-1182 , 2011

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

13

Genetic counseling and "molecular" prenatal diagnosis of ho..:

Mercier, Sandra ; Dubourg, Christèle ; Belleguic, Marion...
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 154C (2010) 1 - p. 191-196 , 2010

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

14

Identification of gene copy number variations in patients w..:

Jaillard, Sylvie ; Drunat, Séverine ; Bendavid, Claude...
European Journal of Medical Genetics. 53 (2010) 2 - p. 66-75 , 2010

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

15

Twelve new patients with 13q deletion syndrome: Genotype–ph..:

Quélin, Chloé ; Bendavid, Claude ; Dubourg, Christèle...
European Journal of Medical Genetics. 52 (2009) 1 - p. 41-46 , 2009

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