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Ferechte Encha-Razavi

Showing results (1-10 of 19) with videos related to

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Brain Research|February 13, 2010
Differential distribution of group I metabotropic glutamate receptors in developing human cortexKarin Boer, Ferechte Encha-Razavi, Martine Sinico, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 23, 2002
Unusual variant of holoprosencephaly in monosomy 13qPascale Marcorelles, Philippe Loget, Catherine Fallet-Bianco, et al.
American Journal of Medical Genetics. Part A|June 10, 2022
Broadening the phenotypic spectrum of TUBA1A tubulinopathy to syndromic arthrogryposis multiplex congenitaMathilde Weber, Dana Jaber, Ferechte Encha-Razavi, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|April 6, 2022
Prenatal Diagnosis of <i>COL4A1</i> Mutations in Eight Cases: Further Delineation of the Neurohistopathological PhenotypeFrancesca Gubana, Christo Christov, Thibault Coste, et al.
Microorganisms|January 30, 2020
Adaptive and Innate Immune Cells in Fetal Human Cytomegalovirus-Infected BrainsYann Sellier, Florence Marliot, Bettina Bessières, et al.
American Journal of Medical Genetics. Part A|July 1, 2005
Diaphanospondylodysostosis (DSD): confirmation of a recessive disorder with abnormal vertebral ossification and nephroblastomatosisMarie Gonzales, Alain Verloes, Marie-Hélène Saint Frison, et al.
Cytogenetic and Genome Research|November 18, 2014
17q21.31 microdeletion: brain anomalies leading to prenatal diagnosisMatthieu Egloff, Ferechte Encha-Razavi, Catherine Garel, et al.
European Journal of Medical Genetics|January 7, 2016
De novo TUBB2B mutation causes fetal akinesia deformation sequence with microlissencephaly: An unusual presentation of tubulinopathyAnnie Laquerriere, Marie Gonzales, Yoann Saillour, et al.
American Journal of Human Genetics|May 16, 2007
Matthew-Wood syndrome is caused by truncating mutations in the retinol-binding protein receptor gene STRA6Christelle Golzio, Jelena Martinovic-Bouriel, Sophie Thomas, et al.
Clinical Genetics|September 14, 2020
Hydrothorax in fetal cases of Opitz G/BBB diagnosis: Extending the phenotype?Aude Tessier, Lucile Boutaud, Ange-Line Bruel, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Brain Research|February 13, 2010
Differential distribution of group I metabotropic glutamate receptors in developing human cortexKarin Boer, Ferechte Encha-Razavi, Martine Sinico, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 23, 2002
Unusual variant of holoprosencephaly in monosomy 13qPascale Marcorelles, Philippe Loget, Catherine Fallet-Bianco, et al.
American Journal of Medical Genetics. Part A|June 10, 2022
Broadening the phenotypic spectrum of TUBA1A tubulinopathy to syndromic arthrogryposis multiplex congenitaMathilde Weber, Dana Jaber, Ferechte Encha-Razavi, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|April 6, 2022
Prenatal Diagnosis of <i>COL4A1</i> Mutations in Eight Cases: Further Delineation of the Neurohistopathological PhenotypeFrancesca Gubana, Christo Christov, Thibault Coste, et al.
Microorganisms|January 30, 2020
Adaptive and Innate Immune Cells in Fetal Human Cytomegalovirus-Infected BrainsYann Sellier, Florence Marliot, Bettina Bessières, et al.
American Journal of Medical Genetics. Part A|July 1, 2005
Diaphanospondylodysostosis (DSD): confirmation of a recessive disorder with abnormal vertebral ossification and nephroblastomatosisMarie Gonzales, Alain Verloes, Marie-Hélène Saint Frison, et al.
Cytogenetic and Genome Research|November 18, 2014
17q21.31 microdeletion: brain anomalies leading to prenatal diagnosisMatthieu Egloff, Ferechte Encha-Razavi, Catherine Garel, et al.
European Journal of Medical Genetics|January 7, 2016
De novo TUBB2B mutation causes fetal akinesia deformation sequence with microlissencephaly: An unusual presentation of tubulinopathyAnnie Laquerriere, Marie Gonzales, Yoann Saillour, et al.
American Journal of Human Genetics|May 16, 2007
Matthew-Wood syndrome is caused by truncating mutations in the retinol-binding protein receptor gene STRA6Christelle Golzio, Jelena Martinovic-Bouriel, Sophie Thomas, et al.
Clinical Genetics|September 14, 2020
Hydrothorax in fetal cases of Opitz G/BBB diagnosis: Extending the phenotype?Aude Tessier, Lucile Boutaud, Ange-Line Bruel, et al.
Pageof 2