E-LIB Suche - Ergebnisse für: Hyon, Capucine

1

CO6-1 Exceptionnelle découverte de quatre phénotypes érythr..:

Peyrard, Thierry ; Florent, Martine ; Sardnal, Véronique...
Transfusion Clinique et Biologique. 30 (2023) - p. S48 , 2023

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

2

L19-3 Réunions de concertation pluridisciplinaire en situat..:

Chami, Btissam ; Hyon, Capucine ; Peyrard, Thierry
Transfusion Clinique et Biologique. 30 (2023) - p. S19 , 2023

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

3

SRY‐negative 46,XX testicular/ovotesticular DSD: Long‐term ..:

Lambert, Sophie ; Peycelon, Matthieu ; Samara‐Boustani, Dinane...
Clinical Endocrinology. 94 (2020) 4 - p. 667-676 , 2020

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

4

A Novel 3q29 Deletion in Association With Developmental Del..:

Chirita Emandi, Adela ; Dobrescu, Andreea Iulia ; Doros, Gabriela...
Frontiers in Pediatrics. 7 (2019) - p. , 2019

Link: https://doi.org/10.3389/..

5

Mutations involving the SRY-related gene SOX8 are associate..:

Portnoi, Marie-France ; Dumargne, Marie-Charlotte ; Rojo, Sandra...
Human Molecular Genetics. 27 (2018) 7 - p. 1228-1240 , 2018

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

6

Loss of Function of the Nuclear Receptor NR2F2, Encoding CO..:

Bashamboo, Anu ; Eozenou, Caroline ; Jorgensen, Anne...
The American Journal of Human Genetics. 102 (2018) 3 - p. 487-493 , 2018

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

7

Inversion péricentrique d'un chromosome 7 associée à une in..:

Hyon, Capucine ; Grouthier, Virginie ; Dournaux, Patricia...
Morphologie. 100 (2016) 330 - p. 162 , 2016

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

8

Nuclear volume differences between balanced and unbalanced ..:

Rouen, Alexandre ; Lavillaureix, Alinoë ; Hyon, Capucine...
Reproductive BioMedicine Online. 30 (2015) 3 - p. 290-295 , 2015

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

9

Refining the regulatory region upstream of SOX9 associated ..:

Hyon, Capucine ; Chantot‐Bastaraud, Sandra ; Harbuz, Radu...
American Journal of Medical Genetics Part A. 167 (2015) 8 - p. 1851-1858 , 2015

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

10

Xp21 deletion in female patients with intellectual disabili..:

Heide, Solveig ; Afenjar, Alexandra ; Edery, Patrick...
European Journal of Medical Genetics. 58 (2015) 6-7 - p. 341-345 , 2015

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

11

First Birth after Sperm Selection through Discontinuous Gra..:

Rouen, Alexandre ; Hyon, Capucine ; Balet, Richard...
Case Reports in Genetics. 2014 (2014) - p. 1-2 , 2014

Link: https://doi.org/10.1155/..

12

Are human male patients with DAX1/NR0B1 mutations infertile:

Ravel, Célia ; Hyon, Capucine ; Siffroi, Jean-Pierre.
Annales d'Endocrinologie. 75 (2014) 2 - p. 126-127 , 2014

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

13

Simultaneous cell by cell study of both DNA fragmentation a..:

Rouen, Alexandre ; Pyram, Ketty ; Pollet-Villard, Xavier...
Journal of Assisted Reproduction and Genetics. 30 (2013) 3 - p. 383-390 , 2013

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

14

Familial Turner syndrome with an X;Y translocation mosaicis..:

Portnoï, Marie-France ; Chantot-Bastaraud, Sandra ; Christin-Maitre, Sophie...
European Journal of Medical Genetics. 55 (2012) 11 - p. 635-640 , 2012

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

15

A new 17p13.3 microduplication including the PAFAH1B1 and Y..:

Hyon, Capucine ; Marlin, Sandrine ; Chantot-Bastaraud, Sandra...
European Journal of Medical Genetics. 54 (2011) 3 - p. 287-291 , 2011

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