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Kherraf, Zine‐Eddine
164
results:
Search for persons
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Format
Online (164)
Mediatypes
Articles (Online) (31)
OpenAccess-fulltext (133)
Languages
english (161)
french (3)
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1
Phenotypic continuum and poor intracytoplasmic sperm inject..:
Wehbe, Zeina
;
Barbotin, Anne‐Laure
;
Boursier, Angèle
...
Andrology. , 2024
Link:
https://doi.org/10.1111/..
?
2
Whole genome sequencing identifies a homozygous splicing va..:
Amiri‐Yekta, Amir
;
Sen, Sharanya
;
Hazane‐Puch, Florence
...
Clinical Genetics. , 2024
Link:
https://doi.org/10.1111/..
?
3
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/..
?
4
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/..
?
5
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/..
?
6
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/..
?
7
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/..
?
8
Overview of the Genetic Causes of Hereditary Breast and Ova..:
Bouras, Ahmed
;
Guidara, Souhir
;
Leone, Mélanie
...
Cancers. 15 (2023) 13 - p. 3420 , 2023
Link:
https://doi.org/10.3390/..
?
9
A recurrent ZP1 variant is responsible for oocyte maturatio..:
Loeuillet, Corinne
;
Dhellemmes, Magali
;
Cazin, Caroline
...
Clinical Genetics. 102 (2022) 1 - p. 22-29 , 2022
Link:
https://doi.org/10.1111/..
?
10
Oligogenic heterozygous inheritance of sperm abnormalities ..:
Martinez, Guillaume
;
Coutton, Charles
;
Loeuillet, Corinne
...
eLife. 11 (2022) - p. , 2022
Link:
https://doi.org/10.7554/..
?
11
Identification and Characterization of an Exonic Duplicatio..:
Bouras, Ahmed
;
Lafaye, Cyril
;
Leone, Melanie
...
International Journal of Molecular Sciences. 23 (2022) 2 - p. 667 , 2022
Link:
https://doi.org/10.3390/..
?
12
A missense mutation in IFT74, encoding for an essential com..:
Lorès, Patrick
;
Kherraf, Zine-Eddine
;
Amiri-Yekta, Amir
...
Human Genetics. 140 (2021) 7 - p. 1031-1043 , 2021
Link:
https://doi.org/10.1007/..
?
13
KH domain containing 3 like (KHDC3L) frame-shift mutation c..:
Fatemi, Nayeralsadat
;
Ray, Pierre F.
;
Ramezanali, Fariba
...
European Journal of Obstetrics & Gynecology and Reproductive Biology. 259 (2021) - p. 100-104 , 2021
Link:
https://doi.org/10.1016/..
?
14
Correction to: A missense mutation in IFT74, encoding for a..:
Lorès, Patrick
;
Kherraf, Zine-Eddine
;
Amiri-Yekta, Amir
...
Human Genetics. 140 (2021) 7 - p. 1045-1045 , 2021
Link:
https://doi.org/10.1007/..
?
15
Leucine zipper transcription factor-like 1 (LZTFL1), an int..:
Huang, Qian
;
Li, Wei
;
Zhou, Qi
...
Developmental Biology. 477 (2021) - p. 164-176 , 2021
Link:
https://doi.org/10.1016/..
1-15