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Author/Creator Grotto, S.

1. EP23.06: Prenatal diagnosis of Fontaine progeroid syndrome with a de novo mutation in SLC25A24. (14th September 2022)

Authors:
Pannier, E.; Roux, N.; Boutaud, L.; Grotto, S.; Molac, C.; El Khattabi, L.; Ichkou, A.; Fourrage, C.; Razavi, F.; Menzella, D.; Grangé, G.; Thébault, F.; Bernabé‐Dupont, C.; Lohmann, L.; Goffinet, F.; Tsatsaris, V.; Attie‐Bitach, T.
Journal:
Ultrasound in obstetrics & gynecology
Issue:
Volume 60(2022)Supplement 1
Page Start:
186
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorder. Issue 2 (10th July 2018)

Authors:
Lévy, J.; Grotto, S.; Mignot, C.; Maruani, A.; Delahaye‐Duriez, A.; Benzacken, B.; Keren, B.; Haye, D.; Xavier, J.; Heulin, M.; Charles, E.; Verloes, A.; Dupont, C.; Pipiras, E.; Tabet, A.‐C.
Journal:
Clinical genetics
Issue:
Volume 94:Issue 2(2018)
Page Start:
264
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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