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

1

Photosensitized degradation of terbuthylazine in water:

Sanlaville, Y. ; Guittonneau, S. ; Mansour, M....
Chemosphere. 33 (1996) 2 - p. 353-362 , 1996

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

2

Capillary electrophoretic study of atrazine photolysis:

Schmitt, Ph. ; Freitag, D. ; Sanlaville, Y...
Journal of Chromatography A. 709 (1995) 1 - p. 215-225 , 1995

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

3

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/..

4

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/..

5

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/..

6

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/..

7

Chromosomal contacts connect loci associated with autism, B..:

2p15 Consortium ; Loviglio, M N ; Leleu, M...
Molecular Psychiatry. 22 (2016) 6 - p. 836-849 , 2016

Link: https://doi.org/10.1038/..

8

Refining the phenotypical and mutational spectrum of Taybi‐..:

Putoux, A. ; Alqahtani, A. ; Pinson, L....
Clinical Genetics. 90 (2016) 6 - p. 550-555 , 2016

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

9

Study of six patients with completeF9deletion characterized..:

Jourdy, Y. ; Chatron, N. ; Carage, M.-L....
Journal of Thrombosis and Haemostasis. 14 (2016) 10 - p. 1988-1993 , 2016

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

10

SFRP-11 – Recherche clinique – Remaniement complexe du chro..:

Putoux, A. ; Andre, J.M. ; Till, M....
Archives de Pédiatrie. 15 (2008) 5 - p. 1034 , 2008

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

11

Familial CHARGE syndrome because of CHD7 mutation: clinical..:

Delahaye, A ; Sznajer, Y ; Lyonnet, S...
Clinical Genetics. 72 (2007) 2 - p. 112-121 , 2007

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

12

Clinical overlap of OFD type IX with Pallister–Killian synd..:

Geneviève, D. ; Sznajer, Y. ; Raoul, M....
American Journal of Medical Genetics Part A. 122A (2003) 2 - p. 180-182 , 2003

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

13

Phenotypic spectrum and transcriptomic profile associated w..:

Castilla-Vallmanya, Laura ; Selmer, Kaja K ; Dimartino, Clémantine...
https://research.rug.nl/en/publications/8e8998ec-ccaa-455e-a596-da5510dffa04. , 2020

Link: https://hdl.handle.net/1..

14

Phenotypic spectrum and transcriptomic profile associated w..:

Castilla-Vallmanya, Laura ; Selmer, Kaja K ; Dimartino, Clémantine...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8093014/. , 2020

Link: http://www.ncbi.nlm.nih...

15

Quantifying the Effects of 16p11.2 Copy Number Variants on ..:

Martin-Brevet, Sandra ; Rodríguez-Herreros, Borja ; Nielsen, Jared A...
info:eu-repo/semantics/altIdentifier/pmid/29778275. , 2018

Link: http://hdl.handle.net/23..