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Author/Creator Encha-Razavi, Férechté

3. Novel KIF7 mutations extend the phenotypic spectrum of acrocallosal syndrome. Issue 11 (2nd November 2012)

Authors:
Putoux, Audrey; Nampoothiri, Sheela; Laurent, Nicole; Cormier-Daire, Valérie; Beales, Philip L; Schinzel, Albert; Bartholdi, Deborah; Alby, Caroline; Thomas, Sophie; Elkhartoufi, Nadia; Ichkou, Amale; Litzler, Julie; Munnich, Arnold; Encha-Razavi, Férechté; Kannan, Rajesh; Faivre, Laurence; Bodda...
Journal:
Journal of medical genetics
Issue:
Volume 49:Issue 11(2012)
Page Start:
713
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

4. OTX2 mutations contribute to the otocephaly-dysgnathia complex. Issue 6 (10th May 2012)

Authors:
Chassaing, Nicolas; Sorrentino, Susanna; Davis, Erica E; Martin-Coignard, Dominique; Iacovelli, Anthony; Paznekas, William; Webb, Bryn D; Faye-Petersen, Ona; Encha-Razavi, Férechté; Lequeux, Leopoldine; Vigouroux, Adeline; Yesilyurt, Ahmet; Boyadjiev, Simeon A; Kayserili, Hülya; Loget, Philippe; ...
Journal:
Journal of medical genetics
Issue:
Volume 49:Issue 6(2012)
Page Start:
373
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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