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Férechté Encha-Razavi

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Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|June 13, 2003
Identification of brain malformations: neuropathological approachFérechté Encha-Razavi
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|June 27, 2003
Features of the developing brainFérechté Encha-Razavi, Pascale Sonigo
Birth Defects Research|October 6, 2022
Delineating septo-optic dysplasiaMark Lubinsky, Férechté Encha-Razavi
American Journal of Medical Genetics. Part A|January 19, 2007
Reassessment of holoprosencephaly-diencephalic hamartoblastoma (HDH) associationMarco Castori, Sofia Douzgou, Evelina Silvestri, et al.
Fetal and Pediatric Pathology|September 3, 2005
The spectrum of type III lissencephaly: a clinicopathological updateFabienne Allias, Annie Buenerd, Raymonde Bouvier, et al.
Prenatal Diagnosis|October 27, 2004
Prenatal diagnosis of primary anophthalmia with a 3q27 interstitial deletion involving SOX2Agnès Guichet, Stéphane Triau, Catherine Lépinard, et al.
American Journal of Medical Genetics. Part A|January 16, 2007
Germinal mosaicism and familial recurrence of a SOX2 mutation with highly variable phenotypic expression extending from AEG syndrome to absence of ocular involvementNicolas Chassaing, Brigitte Gilbert-Dussardier, Florence Nicot, et al.
Mechanisms of Development|August 15, 2002
Expression of the SMADIP1 gene during early human developmentYolanda Espinosa-Parrilla, Jeanne Amiel, Joëlle Augé, et al.
American Journal of Medical Genetics|September 5, 2002
Mosaic trisomy 9 and lobar holoprosencephalyMarion Gérard-Blanluet, Claude Danan, Martine Sinico, et al.
Prenatal Diagnosis|January 11, 2008
Prenatal diagnosis of a ring chromosome 14 in a fetus with a severe skeletal dysplasiaGeneviève Quenum-Miraillet, Valérie Malan, Jelena Martinovic, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|June 13, 2003
Identification of brain malformations: neuropathological approachFérechté Encha-Razavi
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery|June 27, 2003
Features of the developing brainFérechté Encha-Razavi, Pascale Sonigo
Birth Defects Research|October 6, 2022
Delineating septo-optic dysplasiaMark Lubinsky, Férechté Encha-Razavi
American Journal of Medical Genetics. Part A|January 19, 2007
Reassessment of holoprosencephaly-diencephalic hamartoblastoma (HDH) associationMarco Castori, Sofia Douzgou, Evelina Silvestri, et al.
Fetal and Pediatric Pathology|September 3, 2005
The spectrum of type III lissencephaly: a clinicopathological updateFabienne Allias, Annie Buenerd, Raymonde Bouvier, et al.
Prenatal Diagnosis|October 27, 2004
Prenatal diagnosis of primary anophthalmia with a 3q27 interstitial deletion involving SOX2Agnès Guichet, Stéphane Triau, Catherine Lépinard, et al.
American Journal of Medical Genetics. Part A|January 16, 2007
Germinal mosaicism and familial recurrence of a SOX2 mutation with highly variable phenotypic expression extending from AEG syndrome to absence of ocular involvementNicolas Chassaing, Brigitte Gilbert-Dussardier, Florence Nicot, et al.
Mechanisms of Development|August 15, 2002
Expression of the SMADIP1 gene during early human developmentYolanda Espinosa-Parrilla, Jeanne Amiel, Joëlle Augé, et al.
American Journal of Medical Genetics|September 5, 2002
Mosaic trisomy 9 and lobar holoprosencephalyMarion Gérard-Blanluet, Claude Danan, Martine Sinico, et al.
Prenatal Diagnosis|January 11, 2008
Prenatal diagnosis of a ring chromosome 14 in a fetus with a severe skeletal dysplasiaGeneviève Quenum-Miraillet, Valérie Malan, Jelena Martinovic, et al.
Pageof 4