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Ghesh, Leila
6  Ergebnisse:
Personensuche X
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1

A Gardos channelopathy associated with nonimmune hydrops an..:

Ghesh, Leïla ; Besnard, Thomas ; Joubert, Madeleine...
Clinical Genetics.  102 (2022)  6 - p. 543-547 , 2022
Link: https://doi.org/10.1111/..
 
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2

Perinatal presentations of non‐immune hydrops fetalis due t..:

Ghesh, Leïla ; Désir, Julie ; Haye, Damien...
Clinical Genetics.  103 (2022)  5 - p. 560-565 , 2022
Link: https://doi.org/10.1111/..
 
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3

The first twonon‐FinnishHYLS1variants: Expanding the phenot..:

Ghesh, Leïla ; Musquer, Marie Denis ; Devisme, Louise...
Clinical Genetics.  100 (2021)  4 - p. 462-467 , 2021
Link: https://doi.org/10.1111/..
 
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4

Novel interstitial 2q12.3q13 microdeletion predisposes to d..:

Huynh, Minh-Tuan ; Beneteau, Claire ; Marion, Gerard...
Molecular Genetics and Metabolism.  132 (2021)  - p. S222-S224 , 2021
Link: https://doi.org/10.1016/..
 
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5

Novel interstitial 2q12.3q13 microdeletion predisposes to d..:

Huynh, Minh-Tuan ; Gérard, Marion ; Ranguin, Kara...
neurogenetics.  22 (2021)  3 - p. 195-206 , 2021
Link: https://doi.org/10.1007/..
 
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6

Autosomal recessive Treacher Collins syndrome due to POLR1C..:

Ghesh, Leila ; Vincent, Marie ; Delemazure, Anne‐Sophie...
American Journal of Medical Genetics Part A.  179 (2019)  7 - p. 1390-1394 , 2019
Link: https://doi.org/10.1002/..
 
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