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Author/Creator Julia, S

1. AB1206-HPR Adaptation into spanish of the scleroderma health assesment questionnaire (S-HAQ). (15th June 2017)

Authors:
Quevedo, P; Rivero, MA; Perez, N; Laborde, H; Earsman, G; Mayer, M; Papasidero, S; Julia, S; Zaffarana, C; Maldonado, R; Khoury, M; Lara, M; Castell, C; Curti, A; Barreira, JC; Steen, V
Journal:
Annals of the rheumatic diseases
Issue:
Volume 76(2017)Supplement 2
Page Start:
1534
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. Molecular characterisation of a ring chromosome 22 in a patient with severe language delay: a contribution to the refinement of the subtelomeric 22q deletion syndrome. Issue 4 (1st April 2002)

Authors:
De Mas, P; Chassaing, N; Chaix, Y; Vincent, M-C; Julia, S; Bourrouillou, G; Calvas, P; Bieth, E
Journal:
Journal of medical genetics
Issue:
Volume 39:Issue 4(2002)
Page Start:
e17
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disability. (18th March 2013)

Authors:
Callier, P; Aral, B; Hanna, N; Lambert, S; Dindy, H; Ragon, C; Payet, M; Collod‐Beroud, G; Carmignac, V; Delrue, MA; Goizet, C; Philip, N; Busa, T; Dulac, Y; Missotte, I; Sznajer, Y; Toutain, A; Francannet, C; Megarbane, A; Julia, S
Journal:
Clinical genetics
Issue:
Volume 84:Number 6(2013:Dec.)
Page Start:
507
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗