E-LIB Suche - Ergebnisse für: Mary, Laura

1

Functional Assessment of a New PBX1 Variant in a 46,XY Fetu..:

Mary, Laura ; Leclerc, Delphine ; Labalme, Audrey...
Genes. 14 (2023) 2 - p. 273 , 2023

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

2

Insuffisance ovarienne prématurée sévère : pensez aux homme..:

Lokchine, Anna ; Mary, Laura ; Launay, Erika...
Morphologie. 107 (2023) 359 - p. 100622 , 2023

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

3

Harassment, assault, bullying and intimidation (HABI) in ar..:

Coltofean-Arizancu, Laura ; Gaydarska, Bisserka ; Plutniak, Sébastien...
Antiquity. 97 (2023) 393 - p. 726-744 , 2023

Link: https://doi.org/10.15184..

4

Infertilité masculine et féminine liés à SYCE1 : cas d'une ..:

Lokchine, Anna ; Launay, Erika ; Nouyou, Bénédicte...
Morphologie. 107 (2023) 359 - p. 100636 , 2023

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

5

Prenatal phenotype of 22q11 micro-duplications: A systemati..:

Mary, Laura ; Lavillaureix, Alinoë ; Perrot, Adélie...
European Journal of Medical Genetics. 65 (2022) 2 - p. 104422 , 2022

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

6

The TALE never ends: A comprehensive overview of the role o..:

Mary, Laura ; Leclerc, Delphine ; Gilot, David..
Human Mutation. 43 (2022) 9 - p. 1125-1148 , 2022

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

7

Phénotype prénatal des microduplications 22q11 : descriptio..:

Mary, Laura ; Lavillaureix, Alinoë ; Perrot, Adélie...
Morphologie. 106 (2022) 354 - p. S19 , 2022

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

8

Archéologie féministe : histoire, politique et actions (Nor..:

Algrain, Isabelle ; Mary, Laura ; Pasquini, Béline.
Les Nouvelles de l'archéologie. , 2022

Link: https://doi.org/10.4000/..

9

Pathogenic variants in KCNQ2 cause intellectual deficiency ..:

Mary, Laura ; Nourisson, Elsa ; Feger, Claire...
American Journal of Medical Genetics Part A. 185 (2021) 6 - p. 1803-1815 , 2021

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

10

Le facteur de transcription PBX1 est responsable d'anomalie..:

Mary, Laura ; Bigand, Antoine ; Cauchoix, Aurélie...
Morphologie. 105 (2021) 350 - p. S3-S4 , 2021

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

11

Terminal 6q deletions cause brain malformations, a phenotyp..:

Lesieur‐Sebellin, Marion ; Till, Marianne ; Khau Van Kien, Philippe...
Prenatal Diagnosis. 42 (2021) 1 - p. 118-135 , 2021

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

12

How citizen scientists contribute to monitor protected area..:

Bonnet, Pierre ; Joly, Alexis ; Faton, Jean‐Michel...
Ecological Solutions and Evidence. 1 (2020) 2 - p. , 2020

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

13

Identification and Characterization of Known Biallelic Muta..:

Schaefer, Elise ; Delvallée, Clarisse ; Mary, Laura...
Frontiers in Genetics. 10 (2019) - p. , 2019

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

14

Bardet‐Biedl syndrome: Antenatal presentation of forty‐five..:

Mary, Laura ; Chennen, Kirsley ; Stoetzel, Corinne...
Clinical Genetics. 95 (2019) 3 - p. 384-397 , 2019

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

15

Genetic kinship and admixture in Iron Age Scytho-Siberians:

Mary, Laura ; Zvénigorosky, Vincent ; Kovalev, Alexey...
Human Genetics. 138 (2019) 4 - p. 411-423 , 2019

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