E-LIB Suche - Ergebnisse für: Coutton, Charles

1

BRCA1 Intragenic Duplication Combined with a Likely Pathoge..:

Ea, Vuthy ; Berthozat, Claudine ; Dreyfus, Hélène...
International Journal of Molecular Sciences. 25 (2024) 11 - p. 6274 , 2024

Link: https://doi.org/10.3390/..

2

Lack of CCDC146, a ubiquitous centriole and microtubule-ass..:

Kherraf, Zine Eddine ; Muroňová, Jana ; Giordani, Elsa...
eLife. 12 (2024) - p. , 2024

Link: https://doi.org/10.7554/..

3

Lack of CCDC146, a ubiquitous centriole and microtubule-ass..:

Kherraf, Zine Eddine ; Muroňová, Jana ; Giordani, Elsa...
eLife. 12 (2024) - p. , 2024

Link: https://doi.org/10.7554/..

4

Familial KCNQ2 mutation: a psychiatric perspective:

Iftimovici, Anton ; Charmet, Angeline ; Desnous, Béatrice...
Psychiatric Genetics. 34 (2023) 1 - p. 24-27 , 2023

Link: https://doi.org/10.1097/..

5

Results and perinatal outcomes from 189 ICSI cycles of coup..:

Boursier, Angèle ; Boudry, Augustin ; Mitchell, Valérie...
Reproductive BioMedicine Online. 47 (2023) 5 - p. 103328 , 2023

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

6

Cytochalasin D restores nuclear size acting on F-actin and ..:

Martinez, Guillaume ; Cappetta, Donato ; Telesca, Marialucia...
International Journal of Biological Sciences. 19 (2023) 7 - p. 2234-2255 , 2023

Link: https://doi.org/10.7150/..

7

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/..

8

Identification of IQCH as a calmodulin-associated protein r..:

Cavarocchi, Emma ; Sayou, Camille ; Lorès, Patrick...
iScience. 26 (2023) 8 - p. 107354 , 2023

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

9

Bypassing Mendel's First Law: Transmission Ratio Distortion..:

Friocourt, Gaëlle ; Perrin, Aurore ; Saunders, Paul A....
International Journal of Molecular Sciences. 24 (2023) 2 - p. 1600 , 2023

Link: https://doi.org/10.3390/..

10

A splice donor variant of GAS8 induces structural disorgani..:

Kherraf, Zine‐Eddine ; Barbotin, Anne‐Laure ; Martinez, Guillaume...
Clinical Genetics. 105 (2023) 2 - p. 220-225 , 2023

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

11

Sperm Meiotic Segregation Analysis of Reciprocal Translocat..:

Del Llano, Edgar ; Perrin, Aurore ; Morel, Frédéric...
International Journal of Molecular Sciences. 24 (2023) 4 - p. 3664 , 2023

Link: https://doi.org/10.3390/..

12

Expanding the sperm phenotype caused by mutations in SPATA2..:

Martinez, Guillaume ; Metzler‐Guillemain, Catherine ; Cazin, Caroline...
Clinical Genetics. 103 (2023) 5 - p. 612-614 , 2023

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

13

New Mutations in DNHD1 Cause Multiple Morphological Abnorma..:

Martinez, Guillaume ; Barbotin, Anne-Laure ; Cazin, Caroline...
International Journal of Molecular Sciences. 24 (2023) 3 - p. 2559 , 2023

Link: https://doi.org/10.3390/..

14

Evidence for high breakpoint variability in 46, XX, SRY‐pos..:

Capron, Céline ; Januel, Louis ; Vieville, Gaëlle...
Andrology. 10 (2022) 8 - p. 1625-1631 , 2022

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

15

Oligogenic heterozygous inheritance of sperm abnormalities ..:

Martinez, Guillaume ; Coutton, Charles ; Loeuillet, Corinne...
eLife. 11 (2022) - p. , 2022

Link: https://doi.org/10.7554/..